hip endoprosthetics

Hip endoprosthetics

Overview

Primary endoprosthetics
Primary Hip Systems

Our primary hip systems offer a comprehensive portfolio to meet a variety of surgical needs. The combination of short and standard stems, femoral heads, and modern acetabular systems enables flexible surgical solutions based on proven implant designs.

Hip stems      Hip cups       Hip heads

 


ACTINIA® hip stem cementless
ACTINIA® hip stem cemented
ACTINIA® hip stem
cementless with collar

ACTINIA® hip stem

ACTINIA® comprises a range of cementless and cemented hip stem implants. The double-tapered stem shape ensures good primary stability. The flattened neck geometry increases the range of motion. The ACTINIA® hip stem system is on the market since 2012 and has been implanted over 90,000 times since then.

General registry data not related to ACTINIA®:

Cementless stems with collars have a lower risk of stem revisions, aseptic loosening and periprosthetic fractures compared to collarless stems.
Further information: ACTINIA® with collar flyer

- non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
- post-traumatic osteoarthritis
- femoral head and femoral neck fractures
- rheumatoid arthritis

Please refer to the Instructions for Use for a full list of indications. 

  • CCD angle
    • 135° standard and lateralized
    • lateralization without changing the CCD angle
  • cemented
    • implavit®; CoCrMo acc. to ISO 5832-4
  • cementless
    • implatan®; TiAl6V4 acc. to ISO 5832-3
  • cementless
    • implaFix® HA; HA-coating acc. to ISO 13779-2
  • 11 sizes standard
  • 10 sizes lateralized
  • cemented and cementless version
  • additional cementless version with collar
  • taper 12 / 14 mm
    • combinable with ic-heads S-XL
  • CE Marking
  • FDA Approval
ECOFIT® hip stem
cementless
ECOFIT® short stem
cementless
ECOFIT® hip stem 133°
cemented
ECOFIT® hip stem coxa vara cementless

ECOFIT® hip stem

ECOFIT® comprises a range of cementless and cemented hip stem implants. Cementless short stems are also part of the portfolio. Different CCD angles and coating variants offer a variety of treatment options. The ECOFIT® hip stem system is on the market since 2004 and has been implanted over 250,000 times since then.

ECOFIT® short stem

The ECOFIT® short stem is a 35-mm-shorter version of the ECOFIT® hip stem 133°. The proximal area of these two stems is identical. As a result, the ECOFIT® short stem does not follow the traditional short stem philosophy, but is prepared and positioned like a standard stem.

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis
  • femoral head and femoral neck fractures
  • rheumatoid arthritis

For ECOFIT® short stem applies:
Short stem hip prostheses are indicated for younger patients (< 70 years) with good bone quality.

Please refer to the Instructions for Use for a full list of indications. 

  • CCD angle
    • 138° standard and lateralized for ECOFIT® hip stem
    • 133° standard and lateralized for ECOFIT® hip stem 133° and ECOFIT® short stem
    • 123° standard for ECOFIT® hip stem coxa vara
    • lateralization without changing the CCD angle
  • cemented
    • implavit®; CoCrMo acc. to ISO 5832-4
  • cementless
    • implatan®; TiAlV acc. to ISO 5832-3 
  • cemented
    • TiN-coating (optional for 138° stem)
  • cementless
    • implaFix® cpTi-coating
    • implaFix® Duo; cpTi- und HA-coating acc. to ISO 13779-2
  • cemented
    • 6 sizes standard and lateralized
    • surface matt or highly polished
  • cementless
    • 10 sizes standard and lateralized
    • 12 sizes standard and lateralized for ECOFIT® hip stem 133°

The ECOFIT® coxa vara hip stem with a CCD angle of 123° is available only in a standard cementless version with cpTi and HA-coatings and in a standard cemented version with a highly-polished surface.

  • taper 12/14 mm
    • combinable with ic-heads S-XL
    • the cementless ECOFIT® hip stems with a 138° CCD angle are combinable with ic heads up to neck length XXXL.
  • subsider
    • a subsider is available as an option for highly polished stems.
  • CE Marking
  • FDA Approval

ic-straight stem type II

The ic-straight stem type II hip system consists cemented stem implants for primary treatment. The fine structure increases the implant surface area and improves fixation with bone cement. The small proximal collar prevents the stem from subsiding and indicates the implantation depth. 

Combination with ic-heads

As the only cemented ic primary stem, the ic-straight stem type II can be combined with ic-heads up to neck length XXXL.

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis
  • femoral head and femoral neck fractures
  • rheumatoid arthritis

Please refer to the Instructions for Use for a full list of indications. 

  • CCD angle
    • 135° standard and lateralized
    • lateralization without changing the CCD angle
  • implavit®; CoCrMo acc. to ISO 5832-4
  • 10 sizes standard
  • 10 sizes lateralized
  • taper 12/14 mm
    • combinable with ic-heads S-XXXL
  • CE Marking

     

ECOFIT® hip cup

ECOFIT® is a system of cementless, hemi-spherical, pole-flattened hip cup implants. In addition to polyethylene and ceramic inserts the ECOFIT® cup insert consisting of CoCrMo is also available. Together with the PE heads of the ECOFIT® 2M system it enables a tripolar treatment. The ECOFIT® hip cup system is on the market since 2007 and has been implanted over 130,000 times since then.

Triradial design

Pole area: flattened pole
Fit area: reaming corresponds to cup geometry
Press-fit area: underreaming in the peripheral area

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis
  • treatment of fractures that are unmanageable using other surgical techniques
  • rheumatoid arthritis

The ECOFIT® insert is indicated for patients with an increased risk of dislocation.

Please refer to the Instructions for Use for a full list of indications. 

3 holes (sealed with crunch plugs)
To increase primary stability, the plugs anchored in the cup can be removed and the screw holes can be filled with cancellous bone screws Ø 6.5 mm (15 - 80 mm). Cancellous bone screws can be inserted at an angle of up to 15°.

  • implatan®; TiAl6V4 acc. to ISO 5832-3
  • implaFix®; cpTi-coating
  • implaFix® Duo; cpTi- und HA-coating acc. to ISO 13779-2
  • 12 sizes Ø 46 - 68 mm
     
  • insert options
    • polyethylene (UHMW-PE, implacross®, implacross® E): 0° and 10°
    • BIOLOX® delta ceramic
    • ECOFIT® insert (dual mobility)
  • Treatment using a PE cup insert with a 36 mm femoral head is possible for acetabular cup sizes starting from 50 mm.
  • Dual mobility treatment using the ECOFIT® insert is possible for acetabular cup sizes starting from 50 mm.
  • CE Marking
  • FDA Approvals

ECOFIT® cup EPORE® 

ECOFIT® EPORE® is a system of cementless, hemi-spherical, pole-flattened hip cup implants. In addition to polyethylene and ceramic inserts the ECOFIT® insert consisting of CoCrMo is also available. Together with the PE heads of the ECOFIT® 2M system it enables a tripolar treatment. The ECOFIT® cup EPORE® system is on the market since 2016 and has been implanted over 75,000 times since then.

Triradial design

Pole area: flattened pole 
Fit area: reaming corresponds to cup geometry
Press-fit area: underreaming in the peripheral area

EPORE®

EPORE® is an additively manufactured, highly porous structure made of titanium alloy (TiAl6V4). It is very similar to bone structure, like other porous materials and probably thus favors the ingrowth of the implant into the bone.

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis,
  • post-traumatic osteoarthritis,
  • treatment of fractures that are unmanageable using other surgical techniques,  
  • rheumatoid arthritis,
  • revision hip arthroplasty

The ECOFIT® insert is indicated for patients with an increased risk of dislocation.

Please refer to the Instructions for Use for a full list of indications. 

3 or 7 holes (sealed with crunch plugs)
To increase primary stability, the plugs anchored in the cup can be removed and the screw holes can be filled with cancellous bone screws Ø 6.5 mm (15 - 80 mm). Cancellous bone screws can be inserted at an angle of up to 15°.

  • TiAl6V4 with EPORE®
  • 16 sizes Ø 42-72 mm
  • 3 holes / 7 holes (MH Multihole)
     
  • insert options
    • polyethylene (UHMW-PE, implacross®, implacross® E): 0° and 10°
    • BIOLOX® delta ceramic
    • ECOFIT® insert (dual mobility)
  • Treatment using a PE cup insert with a 36 mm femoral head is possible for acetabular cup sizes starting from 50 mm.
  • Dual mobility treatment using the ECOFIT® insert is possible for acetabular cup sizes starting from 50 mm.
  • CE Marking

ECOFIT® SC screw cup

ECOFIT® SC is a hemi-spherical screw-in cup. In addition to its rough-blasted surface, the system is characterized by its modular design. This allows the use of various cup inserts with the screw cup.

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis
  • treatment of fractures that are unmanageable using other surgical techniques
  • rheumatoid arthritis

Please refer to the Instructions for Use for a full list of indications. 

  • cementless screw-in anchorage
    • Using special instruments, the teeth of the ECOFIT® SC  screw cup are screwed into the bone.
  • implatan®; TiAl6V4 acc. to ISO 5832-3

12 sizes Ø 46-68 mm

  • insert options
    • Polyethylene (UHMW-PE, implacross®, implacross® E): 0° and 10°
    • BIOLOX® delta ceramic

Treatment using a PE cup insert with a 36 mm femoral head is possible for acetabular cup sizes starting from 50 mm.

  • CE Marking

     

Mueller II PE hip cup implacross® E
Mueller II PE hip cup

Mueller II PE hip cup

The Mueller II PE hip cup system comprises a range of cemented polyethylene acetabular implants. The cement grooves increase the implant surface area and improve anchorage in the bone cement. Radiopacity is ensured by X-ray wire.
The Mueller II acetabular system is on the market since 1998 and has already been implanted over 75,000 times since then.

Variety of options

In addition to the standard Mueller II PE hip cup, cups with a snap-fit mechanism and dysplasia cups with a 10° unilateral cranial roof are also available. Mueller II PE hip cups made of implacross® E (cross-linked polyethylene with vitamin E) are also available. 

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis,
  • post-traumatic osteoarthritis,
  • treatment of fractures that are unmanageable using other surgical techniques
  • rheumatoid arthritis

Please refer to the Instructions for Use for a full list of indications.

  • Mueller II PE hip cup
    • for small acetabula from cup size 40 mm
  • Mueller II PE hip cup dysplasia 10°
    • Roofing to reduce the risk of dislocation
  • Mueller II PE hip cup snap
    • slight undersize of the cup opening compared to the ic-head ensures that the ic head snaps into place
  • Mueller II PE hip cup implacross® E
    • can be combined with 36 mm ic-heads
  • Mueller II PE hip cup, Mueller II PE hip cup dysplasia 10°, Mueller II PE hip cup snap
    • UHMWPE acc. to ISO 5834-2
  • Mueller II PE hip cup implacross® E
    • implacross® E; crosslinked UHMWPE with Vitamin E
  • Stainless Steel X-ray wire acc. to ISO 5832-1
  • Mueller II PE hip cup
    • Ø 40 - 64 mm for various head diameters
  • Mueller II PE hip cup dysplasia 10°
    • Ø 44 - 64 mm for various head diameters
  • Mueller II PE hip cup snap
    • Ø 44 - 64 mm for head diameter 32 mm
  • Mueller II PE hip cup implacross® E
    • Ø 44 - 64 mm for various head diameters

The Mueller II PE hip cups are compatible with the MUTARS® PRS system.

  • CE Marking

ic bipolar head CoCrMo

The ic bipolar head CoCrMo is used as a bipolar hemiendoprosthesis. The outer shell of the bipolar head is highly polished and comes pre-assembled with a polyethylene liner and a retaining ring. The ic bipolar head is on the market since 1998 and has been implanted over 150,000 times since then.

The main indications for the insertion of a hemi arthroplasty implant (Bipolar or Unipolar head):

  • femoral neck fractures
  • femoral head necrosis

Please refer to the Instructions for Use for a full list of indications. 

The ic bipolar head CoCrMo articulates directly with the natural acetabulum.

  • outer shell
    • implavit®; CoCrMo acc. to ISO 5832-4
  • insert and locking ring
    • UHMWPE acc. to ISO 5834-2
  • 24 sizes
  • outer shell Ø 38 - 62 mm
  • combination
    • Ø 38-41 mm combinable with Ø 22 mm heads
    • Ø 42-62 mm combinable with Ø 28 mm heads
  • CE Marking
  • FDA Approvals
ic-head BIOLOX® delta
ic-head CoCrMo
ic-head Titan

ic-heads

In hip systems, the heads function as the articulation partner between the acetabular component and the hip stem. They are connected to the hip stem via a taper. The metallic ic-heads made of titanium and CoCrMo are designed for articulation with polyethylene components in total or hemi-hip arthroplasty. In addition to polyethylene components, the ceramic ic-heads BIOLOX® delta are also compatible with BIOLOX® delta cup inserts, thus creating a ceramic-on-ceramic articulation.

ic-head titanium

The ic-head titanium is made of implatan® TiAl6V4 and is coated with a ceramic TiN coating.

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis
  • Femoral neck fracture
  • rheumatoid arthritis
     
  • Indications for the application of hip heads:
    • primary total hip arthroplasty of the hip joint affected by arthrosis
    • revision hip arthroplasty

Please refer to the Instructions for Use for a full list of indications. 

  • taper 12 / 14 mm

neck lenght: 
ic-head titanium and ic-head CoCrMo

 

22 mm

28 mm

32 mm + 36 mm

S

-4 mm

-3,5 mm

-4 mm

M

0 mm

0 mm

0 mm

L

+4 mm

+3,5 mm

+4 mm

XL

 

+7 mm

+8 mm

XXL

 

+10,5 mm

+12 mm

XXXL

 

+14 mm

+16 mm

 

ic-head BIOLOX® delta

 

28 mm

32 mm

36 mm + 40 mm

S

-3,5 mm

-4 mm

-4 mm

M

0 mm

0 mm

0 mm

L

+3,5 mm

+4 mm

+4 mm

XL

 

+7 mm

+8 mm

 

ic-head revision BIOLOX® delta with taper adapter

S

-3 mm

M

0 mm

L

+4 mm

XL

+7 mm

  • ic-head titanium
    • implatan®; TiAl6V4 acc. to ISO 5832-3
  • ic-head CoCrMo
    • implavit®; CoCrMo acc. to ISO 5832-12
  • ic-head BIOLOX® delta
    • Al2O3 and ZrO2 acc. to ISO 6474-2
  • ic-head revision BIOLOX® delta with taper adapter
    • Al2O3 and ZrO2 acc. to ISO 6474-2 and TiAl6V4 acc. to ISO 5832-3 (taper adapter)
  • ic-head titanium
    • TiN-coating
  • ic-head CoCrMo
    • TiN-coating optional for Ø 22 mm heads
  • ic-head titanium
    • Ø 28 / 32 / 36 mm
    • neck length S-XXXL
  • ic-head CoCrMo
    • Ø 22 / 28 / 32 / 36 mm
    • neck length S-XXXL (Ø 22 mm: S-L)
  • ic-head BIOLOX® delta
    • Ø 28 / 32 / 36 / 40 mm
    • neck length S-XL (Ø 28 mm: S-L)
  • ic-head revision BIOLOX® delta
    • Ø 28 / 32 / 36 / 40 mm
    • neck length taper adapter S-XL 
  • The combination of the ic-heads XXL and XXXL is only possible to a limited extent.
  • BIOLOX® is a registered trademark of the company CeramTec.
  • CE Marking
  • FDA Approvals
Revision endoprosthetics
Revision Hip Systems

Our hip revision systems offer comprehensive treatment options for difficult defects and complex revision cases. From stem or cup revisions to complex reconstructive procedures, a wide range of implants is available. Thanks to the proven modularity and compatibility of our MUTARS® system, customized solutions can be created to meet a variety of clinical needs.

Hip stems    Hip cups     


BICANA® hip stem

BICANA® comprises a range of cemented hip stem implants for primary or revision cases. The extensive collar allows physiological proximal load transmission and has a resection angle of 45° to the femoral axis. The BICANA® hip stem system is on the market since 2008 and has been implanted over 30,000 times since then.

BICANA® hip stem revision

For revision cases, stems are available in lengths of 200, 250 and 300 mm.

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis
  • femoral head and femoral neck fractures
  • rheumatoid arthritis

The main indication for BICANA® hip stems revision is Revision hip arthroplasty.

Please refer to the Instructions for Use for a full list of indications. 

  • CCD angle
    • 117°
    • 126°
    • 126° + 10.5 mm
    • 135°
  • length
    • 130 mm
    • 150 mm
    • 200 mm
    • 250 mm
    • 300 mm

S-shaped stem design
The anatomical s-shaped geometry ensures additional stability. A physiological anteversion of 5° is integrated into the head-neck area of the stem.

  • implavit®; CoCrMo nach ISO 5832-4
  • 3 to 6 sizes (depending on the CCD angle and stem length) for both left and right sides
  • taper 12 / 14 mm
    • combinable with ic-heads S-XL
  • CE Marking

DIALOC® RS hip stem

DIALOC® RS comprises a range of cementless hip stem implants for revision cases.
The anatomical design of the calcar region of the stems supports press-fit fixation in the proximal femur.

Stem design

The tapered, rectangular design ensures high rotational and primary stability.

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis
  • femoral head and femoral neck fractures
  • rheumatoid arthritis
     
  • The main indication for DIALOC® RS  revision stem is:
    • revision hip arthroplasty (Paprosky Type I to IIIa)

Please refer to the Instructions for Use for a full list of indications. 

  • CCD angle
    • 131° standard
  • length
    • 181 - 221 mm
  • implatan®; TiAl6Nb7 acc. to ISO 5832-11
  • 8 sizes standard
  • taper 12 / 14 mm
    • combinable with ic-heads S-XXXL
  • CE Marking

MUTARS® RS

The MUTARS® RS revision system bridges proximal femoral bone defects due to fractures or revision arthroplasties. For optimal fit, different sizes are available. The modularity of the components simplifies the optimal filling of the proximal femoral area. The intention is to preserve as much bone substance as possible for sufficient primary stability.

Reconstruction

The MUTARS® RS revision system enables implant lengths of 192–417 mm.

Need for femoral arthroplasty due to femoral defects e.g. caused by:

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis,
  • fractures
  • rheumatoid arthritis
  • revision of loosened femoral prosthesis components with extensive bone resorption of the proximal femur and widening of the medullary cavity or strong thinning of the cortical bone in the proximal region of the femur
  • revision of loosened femoral prosthesis components with periprosthetic or subprosthetic fracture
  • revision of non-loosened femoral prosthesis components with periprosthetic or subprosthetic fracture that cannot be treated in any other way
  • revision surgery in cases of an extensive comminuted fracture in the proximal third of the femur in elderly patients in whom there is an indication for a pros-thetic treatment, but a sufficient fixation of a standard endoprosthesis is not possible.

Please refer to the Instructions for Use for a full list of indications.

  • MUTARS® RS stem cementless
    • length: 150, 200 and 250 mm
    • Ø 12 - 22 mm (in 1 mm steps) for lengths 150 mm and 200 mm
    • Ø 14 - 22 mm (in 1 mm steps) for length 250 mm
  • MUTARS® RS stem cemented
    • length: 120, 150 and 200 mm
    • Ø 12 - 18 mm (in 2 mm steps)
  • MUTARS® RS proximal component
    • length: 32 mm and 42 mm
    • CCD angle: 127° / 135°
  • MUTARS® RS metaphyseal component
    • length: 40 mm and 50 mm
    • size: standard / slim
  • MUTARS® RS extension piece
    • length: 25 mm
  • MUTARS® RS screw
    • length: 40 - 125 mm
    • thread: M8 x 1
  • MUTARS® RS stem cementless
    • implatan®; TiAl6V4 acc. to ISO 5832-3
  • MUTARS® RS stem cemented
    • implavit®; CoCrMo acc. to ISO 5832-4
  • MUTARS® RS proximal component / metaphyseal component / extension piece / screw
    • implatan®; TiAl6V4 acc. to ISO 5832-3
  • MUTARS® RS stem cementless
    • implaFix® HA; HA-coating acc. to ISO 13779-2 (optional)
  • MUTARS® RS stem cemented
    • TiN-coating (optional)
  • MUTARS® RS proximal component
    • Silver-coating (optional)
  • MUTARS® RS metaphyseal component / extension piece
    • implaFix® HA; HA-coating acc. to ISO 13779-2 (optional)
  • MUTARS® RS stem cementless
    • 31 sizes
  • MUTARS® RS stem cemented
    • 12 sizes
  • MUTARS® RS proximal component
    • 4 sizes
  • MUTARS® RS metaphyseal component
    • 4 sizes
  • MUTARS® RS extension piece
    • 1 size
  • MUTARS® RS screw
    • 8 sizes (The appropriate screw must be selected based on the total length of the modular implants.)
  • taper 12 / 14 mm
    • combinable with ic-heads S-XXXL (Please refer to the Instruction for Use for restrictions)
  • weight limit
    • some stem sizes are limited by weight (Please refer to the Instruction for Use for restrictions)
  • screw options
    • 2 distal holes* for concellous screw Ø 4,5 mm (lengths 25 - 60 mm)
      *for cementless stems Ø 15 - 22 mm (length 200 mm) and Ø 17 - 22 mm (length 250 mm)
  • CE Marking

MUTARS® proximal femur revision

The MUTARS® proximal femur revision is a modular reconstruction prosthesis for replacement of the proximal femur with preservation of the greater trochanter. It has been specifically developed for complex revision situations in which anatomical reconstruction and functional stability are of primary importance.

By using various extension pieces, the reconstruction length can be individually adapted to the patient's anatomical conditions and specific clinical requirements. This enables precise restoration of limb length and biomechanics.With the aid of dedicated trochanter plates, the greater trochanter can be preserved and securely fixed to the implant. The EPORE® surface structure supports bone ingrowth and contributes to improved osseous integration. As a result, the functional importance of the greater trochanter, particularly with regard to muscular attachment and hip stability, can be maintained to the greatest extent possible.

Another key feature is the silver coating. The properties of silver are utilized in the coated components to help reduce the risk of infection and increase the longevity of the prosthesis.

  • severe bone defects requiring hip joint replacement
  • high degree of modularity and compatibility
  • rotational adjustment in 5° increments
  • reconstruction length can be individually adjusted using extension pieces and the connecting piece
  • simplified revision procedures through the use of connecting piece
  • cemented, cementless, and modular stem options
  • soft tissue and greater trochanter reattachment facilitated by the EPORE® surface structure and trochanter plate
  • dual mobility options
  • CCD angles: 127° and 135°
  • TiAl6V4 mit EPORE® (MUTARS® proximal femur revision)
  • implatan®; TiAl6V4 nach ISO 5832-3 (extension pieces, connecting piece, cementless stems)
  • implavit®; CoCrMo nach ISO 5832-4 (cemented stems)
  • implaFix® HA; HA acc to ISO 13779-2 (optional for cementless MUTARS® femoral stems)
  • silver coating (optional for proximal femur revision, extension pieces and connecting piece)
  • TiN coating (optional for cemented MUTARS® femoral stems)
  • 4 sizes of the MUTARS® proximal femur revision
    • lenght: 50 mm and 70 mm
    • CCD angles: 127° and 135°
  • 5 MUTARS® extension pieces: 30 mm, 40 mm, 60 mm, 80 mm and 100 mm
  • MUTARS® connecting piece 100 mm
  • MUTARS® modular stem with EPORE® HA collar
  • MUTARS® femur stem
  • reconstruction length ≥ 70 mm
  • CE Marking
  • FDA Approvals

MUTARS® proximal femur

The MUTARS® proximal femur is a modular endoprosthetic system designed for the reconstruction of extensive bone defects in the proximal femur, for example following tumor resections or in complex revision cases.

Its flexible modular design provides the surgeon with intraoperative freedom of decision-making, enabling a situation-specific treatment approach and thereby contributing to optimal clinical outcomes. 
Another key feature is the silver coating. The properties of silver are utilized in the coated components to help reduce the risk of infection and increase the longevity of the prosthesis. In addition, the retention rings provide the option for soft tissue reattachment using an attachment tube.1),2),3)

1) Gosheger G, Hillmann A, Lindner N, Rödl R, Hoffmann C, Bürger H, Winkelmann W. Soft tissue reconstruction of megaprostheses using a trevira tube. Clin Orthop Relat Res. 2001 Dec;(393):264-71. doi: 10.1097/00003086-200112000-00030. PMID: 11764358.
2) Raiss P, Kinkel S, Sauter U, Bruckner T, Lehner B. Replacement of the proximal humerus with MUTARS tumor endoprostheses. Eur J Surg Oncol. 2010 Apr;36(4):371-7. doi: 10.1016/j.ejso.2009.11.001. Epub 2009 Nov 28. PMID: 19945819.
3) Rachbauer AM, Schneider KN, Gosheger G, Deventer N. Endoprosthetic Reconstruction of the Proximal Humerus with an Inverse Tumor Prosthesis. Cancers (Basel). 2023 Nov 8;15(22):5330. doi: 10.3390/cancers15225330. PMID: 38001590; PMCID: PMC10670134.

  • tumors of the proximal femur
  • severe bone defects requiring hip joint replacement
  • high modularity and compatibility
  • rotation adjustment in 5° increments
  • reconstruction length can be individually adjusted using extension sleeves and the connecting piece
  • simplified revision procedures through the modular connecting piece
  • cemented, cementless, and modular stem options available
  • soft-tissue reattachment possible using the attachment tube
  • duo mobility options
  • 140° CCD angle
  • implatan®; TiAl6V4 nach ISO 5832-3 (MUTARS® proximal femur, MUTARS® extension piece, MUTARS® connecting piece, MUTARS® femoral stems cementless)
  • implavit®; CoCrMo nach ISO 5832-4 (MUTARS® femoral stems cemented)
  • implaFix® HA; HA coating nach ISO 13779-2 (optional for MUTARS® femoral stems cementless)
  • silver coating (optional for MUTARS® proximal femur, MUTARS® extension piece, MUTARS® connecting piece)
  • TiN coating (optional for MUTARS® femoral stems cemented)
  • 2 length of MUTARS® proximal femur: 50 mm and 70 mm
  • 5 MUTARS® extention pieces 30 mm, 40 mm, 60 mm, 80 mm and 100 mm
  • MUTARS® connecting piece 100 mm
  • MUTARS® femoral stems
  • reconstruction length ≥ 80 mm
  • CE Marking
  • FDA Approvals

MUTARS® intramedullary total femur replacement with GenuX® MK

The MUTARS® intramedullary total femur replacement with GenuX® MK provides an advanced solution as a so-called through-stem prosthesis, connecting the proximal and distal femur. Developed for the combined revision of the hip and knee joints, this system enables precise adaptation and optimal functionality.

The intramedullary connecting module is fully compatible with all MUTARS® implants for the proximal and distal femur. The modular system architecture allows for flexible intraoperative adaptation to the patient’s individual anatomical and clinical requirements, thereby supporting precise reconstruction and optimized restoration of function. Another feature is the silver coating, which utilizes the properties of silver in the coated components to reduce the risk of infection and increase the service life of the prosthesis.

The MUTARS® intramedullary total femur replacement with GenuX® MK is also available in an HD version. For more information, please follow this link: HD focus page

  •  revision treatment of the hip and knee joint with intramedullary connection
  • fully coupled knee system
  • high degree of modularity and compatibility
  • fixed-bearing polyethylene inserts and mobile-bearing PE inserts with up to 20° of rotation, available in various heights
  • cemented and cementless femoral and tibial components
  • cemented and cementless stem options
  • 360° freely adjustable offset
  • femoral and tibial spacer fixation
  • EPORE® Cones, EPORE® metaphyseal components
  • compatible with cemented MUTARS® patellar resurfacing components
  • implatan®; TiAl6V4 according to ISO 5832-3 (MUTARS® proximal component, MUTARS® metaphyseal component, MUTARS® extension piece, MUTARS® screws, MUTARS® intramedullary connecting modules, MUTARS® offset adapters, MUTARS® spacers, GenuX® MK cementless stems)
  • implavit®; CoCrMo according to ISO 5832-4 (MUTARS® GenuX® MK femur, MUTARS® GenuX® MK tibia, GenuX® MK cemented stems)
  • implavit®; CoCrMo according to ISO 5832-12 (MUTARS® coupling)
  • UHMWPE according to ISO 5834-2 and implacross® E; cross-linked UHMWPE with vitamin E (inserts)
  • TiN coating (optional for MUTARS® femoral and tibial components, GenuX® MK cemented stems)
  • TiNbN coating (optional for MUTARS® coupling)
  • implaFix® HA; HA coating according to ISO 13779-2 (optional for GenuX® MK cementless stems, MUTARS® extension piece and MUTARS® metaphyseal component)
  • silver coating (optional for MUTARS® proximal component, MUTARS® intramedullary connecting modules and spacer)
  • ic heads
  • 4 MUTARS® RS proximal components
    • length: 32 mm and 42 mm
    • CCD angle: 127° / 135°
  • 4 MUTARS® RS metaphyseal components
    • length: 40 mm and 50 mm
    • size: standard / slim
  • MUTARS® RS extension piece 25 mm
  • MUTARS® intramedullary connecting module for GenuX® MK
    • lenght: 120 mm - 440 mm
    • diameter: 15 mm
  • 4 offset adapter options: 0 mm, 2 mm, 4 mm and 6 mm
  • 5 GenuX® MK femur and tibia components: sz. 2 – 6
  • 3 options of MUTARS® coupling: 12.5 mm, 15 mm and 17.5 mm
  • 3 heigths of MUTARS® GenuX® MK PE inserts: 12.5 mm, 15 mm and 17.5 mm
  • MK femur and tibia spacer
  • GenuX® MK stems
  • MUTARS® patellar replacement
  • reconstruction length ≥ 332 mm (femur length)
  • taper 12 / 14 mm: combinable with ic-heads S-XXXL (Please refer to the Instruction for Use for restrictions)
  • CE Marking

MUTARS® intramedullary total femur replacement with MK KRI

The MUTARS® intramedullary total femur replacement with MK KRI provides an advanced solution for combined hip and knee revision procedures. Designed for the replacement of the distal femur, particularly in cases involving the loss of the distal femoral condyles, this system enables precise adaptation and optimal functionality.

The modular system design enables tailored adaptation to a wide range of anatomical situations. In addition, the system is optionally available with a silver coating, which helps reduce the risk of periprosthetic infections and support the long-term functionality of the implant reconstruction.

The MUTARS® intramedullary total femur replacement with MK KRI is also aviable in an HD version. For more information, please follow this link: HD focus page

  • revision treatment of the hip and knee joint with intramedullary connection in cases of distal femoral condyle loss
  • fully coupled knee system
  • high degree of modularity and compatibility
  • fixed-bearing polyethylene inserts and mobile-bearing PE inserts with up to 20° of rotation, available in various heights
  • cemented and cementless tibial components
  • cemented and cementless stem options
  • 360° freely adjustable offset
  • femoral and tibial spacer fixation
  • EPORE® Cones and EPORE® metaphyseal components
  • compatible with cemented MUTARS® patellar resurfacing components
  • implatan®; TiAl6V4 according to ISO 5832-3 (cementless GenuX® MK stems, offset adapters, spacers, MUTARS® RS screws, MUTARS® RS proximal component, MUTARS® RS metaphyseal component, MUTARS® intramedullary connection modules)
  • implavit®; CoCrMo according to ISO 5832-4 (cemented GenuX® MK stems, MUTARS® MOM KRI, MUTARS® GenuX® MK tibia)
  • implavit®; CoCrMo according to ISO 5832-12 (MUTARS® coupling)
  • UHMWPE according to ISO 5834-2 and implacross® E; cross-linked UHMWPE with vitamin E (inserts)
  • TiN coating (optional for MUTARS® femur and tibial components, cemented GenuX® MK stems)
  • TiNbN coating (optional for MUTARS® coupling)
  • implaFix® HA; HA coating according to ISO 13779-2 (optional for cementless GenuX® MK stems, MUTARS® RS extension piece and MUTARS® RS metaphyseal component)
  • silver TiN coating (optional for MUTARS® MOM KRI)
  • silver coating (optional for MUTARS® RS proximal component, MUTARS® intramedullary connecting modules and spacer)
  • ic heads
  • 4 MUTARS® RS proximal components
    • length: 32 mm and 42 mm
    • CCD angle: 127° / 135°
  • 4 MUTARS® RS metaphyseal components
    • length: 40 mm and 50 mm
    • size: standard / slim
  • MUTARS® RS extension piece 25 mm
  • MUTARS® intramedullary connecting module for KRI
    • lenght: 100 mm – 360 mm
    • diameter: 15 mm
  • MUTARS® MOM KRI
  • 4 offset options: 0 mm, 2 mm, 4 mm und 6 mm
  • 5 GenuX® MK tibia components: sz. 2 – 6
  • 3 heights of PE inserts: 12.5 mm, 15 mm und 17.5 mm
  • 3 options of MUTARS® coupling: 12.5 mm, 15 mm und 17.5 mm
  • MUTARS® patella replacement
  • MK tibia spacer
  • GenuX® MK stems
  • reconstruction length ≥ 327 mm (femur length)
  • taper 12 / 14 mm: combinable with ic-heads S-XXXL (Please refer to the Instruction for Use for restrictions)
  • CE Marking
ECOFIT® 2M hip cup
cemented
ECOFIT® 2M hip cup
cementless
ECOFIT® 2M SP hip cup
with spikes
ECOFIT® 2M hip cup
cemented TiN

ECOFIT® 2M system

ECOFIT® 2M comprises a range of cementless and cemented acetabular implants. Due to the tribiological properties, all acetabular cups are made of implavit®, CoCrMo. The ECOFIT® 2M version with spikes (SP) for additional rotation prevention is also available. The ECOFIT® 2M hip cup system is on the market since 2012 and has been implanted over 35,000 times since then. 

Triradial design

Pole area: flattened pole
Fit area: reaming corresponds to cup geometry
Press-fit area: underreaming in the peripheral area

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis
  • treatment of fractures that cannot be treated using other surgical techniques
  • rheumatoid arthritis
  • hip dysplasia
  • in patients with an increased risk of dislocation:
    • revision hip arthroplasty
    • neuromuscular diseases

Please refer to the Instructions for Use for a full list of indications. 

  • dual mobility
    The PE head, which is attached to the conventional ic-head, allows for combined movement between the ic-head and the inner surface of the PE head on the one hand, and between the outer surface of the PE head and the ECOFIT® 2M acetabular cup on the other. This tripolar design reduces the risk of dislocation.
  • roofing
    The unilateral roofing of the ECOFIT® 2M acetabular cup is 8 mm.
  • cementless
    • implavit®; CoCrMo acc. to ISO 5832-4
  • cemented
    • implavit®; CoCrMo acc. to ISO 5832-4
  • cementless
    • implaFix® Duo; cpTi- und HA-coating acc. to ISO 13779-2
  • cemented
    • TiN-coating (optional)
  • ECOFIT® 2M
    • cemented: 11 sizes Ø 44-64 mm
    • cementless: 12 sizes Ø 42-64 mm
  • ECOFIT® 2M SP
    • cementless: 10 sizes Ø 44-62 mm
       
  • PE-head options
    • 2M head implacross® E: crosslinked UHMW-PE with vitamin E
    • ECOFIT® 2M  head: UHMW-PE acc. to ISO 5834-2

The cemented ECOFIT® 2M acetabular cups are compatible with the MUTARS® PRS system.

  • CE Marking

MUTARS® PRS

Pelvic Reconstruction Shell
MUTARS® PRS is a cementless, spherical reconstruction cup with a flattened pole, used for extensive cavitary or segmental acetabular defects classified as Paprosky type 3a a lower. 
The MUTARS® PRS support ring can be used optional and is intended to support the initial stabilization of the MUTARS® PRS until the osseointegration process is complete.

Triradial design:

Pole area: flattened pole 
Fit area: reaming corresponds to cup geometry
Press-fit area: underreaming in the peripheral area

EPORE®

EPORE® is an additively manufactured, highly porous structure made of titanium alloy (TiAl6V4). It is very similar to bone structure, like other porous materials, and probably thus favors the ingrowth of the implant into the bone.

  • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
  • post-traumatic osteoarthritis
  • fractures
  • rheumatoid arthritis
     
  • The following additional indication applies to the hip joint replacement with the MUTARS® PRS:
    • large cavitary or segmental acetabular defects (up to type 3a of Paprosky classification)
       
  • The following indication applies to the hip joint replacement with the MUTARS® PRS reinforcement cage additionally:
    • severe hip dysplasia,
    • osteoporosis,
    • protrusio acetabuli,
    • cystic acetabular roof,
    • revision

Please refer to the Instructions for Use for a full list of indications. 

  • ø 8 mm cancellous screw
    • In addition to nine holes for 6.5 mm cancellous screws (lengths: 15–80 mm), MUTARS® PRS also features three holes for the use of 8 mm cancellous screws in the lengths 40–100 mm.
       
  • Full Pelvis Solution
    • When used in combination with the EPORE® 8 mm acetabular spacers, EPORE® buttress augments, EPORE® shim augments, and the MUTARS® PRS reinforcement cage, the MUTARS® PRS becomes a full pelvis solution.
  • MUTARS® PRS
    • TiAl6V4 with EPORE®
  • MUTARS® PRS reinforcement cage
    • pure titanium (cpTi) acc. to ISO 5832-2
  • MUTARS® PRS
    • 6 sizes Ø 52-72 mm
  • MUTARS® PRS reinforcement cage
    • 4 sizes long right and left (10 holes)
    • 4 sizes short right and left (5 holes)
  • combinable hip cups
    • ECOFIT® 2M hip cup cemented
    • Mueller II PE hip cup

The MUTARS® PRS can be combined with 8 mm EPORE® acetabular spacers, EPORE® buttress augments, EPORE® shim augments, and the ic-restriktor acetabular.

Please refer to the surgical technique for the exact combination options.

  • CE Marking

MUTARS® RS Cup

The MUTARS® RS cup is a modular, spherical revision hip cup with a flattened pole. The back of the cup has a porous EPORE® structure, which promotes osseointegration. Two anatomically shaped flaps enable the cup to be fixed in the vital part of the os coxae.

EPORE®

EPORE® is an additively manufactured, highly porous structure made of titanium alloy (TiAl6V4). It is very similar to bone structure, like other porous materials, and probably thus favors the ingrowth of the implant into the bone.

  • Extensive cavitary or segmental acetabular defects e.g. caused by:
    • non-inflammatory degenerative joint disease including osteoarthri-tis and avascular necrosis
    • post-traumatic osteoarthritis
    • fractures
    • rheumatoid arthritis
    • revision of acetabular cup prosthesis or acetabular reinforcement cages with defects up to type 3a/3b according to Paprosky classi-fication

For the reconstruction of the bone defects the application of allogenic bone grafts may be required when using the MUTARS® RS cup.

Please refer to the Instructions for Use for a full list of indications. 

The distal flap is wedge-shaped and is attached to the ischium. The proximal flap lies on the outer surface of the ilium and is connected to it by screws. For this purpose, cancellous screws bone screws Ø 6.5 mm (15–80 mm) are available.

  • TiAl6V4 with EPORE®
  • 5 sizes Ø 46-62 mm left and right
     
  • Insert options
    • 2M Inlay 15° TiN (dual mobility)
    • implacross PE-Insert 15° neutral 0 mm and Offset 4 mm
  • CE Marking
Tumour endoprosthetics

MUTARS® proximal femur

The MUTARS® proximal femur is a modular endoprosthetic system designed for the reconstruction of extensive bone defects in the proximal femur, for example following tumor resections or in complex revision cases.

Its flexible modular design provides the surgeon with intraoperative freedom of decision-making, enabling a situation-specific treatment approach and thereby contributing to optimal clinical outcomes. 
Another key feature is the silver coating. The properties of silver are utilized in the coated components to help reduce the risk of infection and increase the longevity of the prosthesis. In addition, the retention rings provide the option for soft tissue reattachment using an attachment tube.1),2),3)

1) Gosheger G, Hillmann A, Lindner N, Rödl R, Hoffmann C, Bürger H, Winkelmann W. Soft tissue reconstruction of megaprostheses using a trevira tube. Clin Orthop Relat Res. 2001 Dec;(393):264-71. doi: 10.1097/00003086-200112000-00030. PMID: 11764358.
2) Raiss P, Kinkel S, Sauter U, Bruckner T, Lehner B. Replacement of the proximal humerus with MUTARS tumor endoprostheses. Eur J Surg Oncol. 2010 Apr;36(4):371-7. doi: 10.1016/j.ejso.2009.11.001. Epub 2009 Nov 28. PMID: 19945819.
3) Rachbauer AM, Schneider KN, Gosheger G, Deventer N. Endoprosthetic Reconstruction of the Proximal Humerus with an Inverse Tumor Prosthesis. Cancers (Basel). 2023 Nov 8;15(22):5330. doi: 10.3390/cancers15225330. PMID: 38001590; PMCID: PMC10670134.

  • tumors of the proximal femur
  • severe bone defects requiring hip joint replacement
  • high modularity and compatibility
  • rotation adjustment in 5° increments
  • reconstruction length can be individually adjusted using extension sleeves and the connecting piece
  • simplified revision procedures through the modular connecting piece
  • cemented, cementless, and modular stem options available
  • soft-tissue reattachment possible using the attachment tube
  • duo mobility options
  • 140° CCD angle
  • implatan®; TiAl6V4 nach ISO 5832-3 (MUTARS® proximal femur, MUTARS® extension piece, MUTARS® connecting piece, MUTARS® femoral stems cementless)
  • implavit®; CoCrMo nach ISO 5832-4 (MUTARS® femoral stems cemented)
  • implaFix® HA; HA coating nach ISO 13779-2 (optional for MUTARS® femoral stems cementless)
  • silver coating (optional for MUTARS® proximal femur, MUTARS® extension piece, MUTARS® connecting piece)
  • TiN coating (optional for MUTARS® femoral stems cemented)
  • 2 length of MUTARS® proximal femur: 50 mm and 70 mm
  • 5 MUTARS® extention pieces 30 mm, 40 mm, 60 mm, 80 mm and 100 mm
  • MUTARS® connecting piece 100 mm
  • MUTARS® femoral stems
  • reconstruction length ≥ 80 mm
  • CE Marking
  • FDA Approvals

MUTARS® MK total femur

The MUTARS® MK total femur represents a proven solution for the reconstruction of the entire femur in complex clinical indications and is primarily used following extensive tumor resections as well as in challenging defect and revision cases.

Thanks to its modular design, the system enables precise anatomical adaptation while ensuring a high level of mechanical stability. The individual components can be combined flexibly to optimally meet the patient's specific anatomical and clinical requirements. Another key feature is the silver coating. The properties of silver are utilized in the coated components to help reduce the risk of infection and increase the longevity of the prosthesis.

In addition, the MUTARS® MK total femur is also available in an HD version. For more information, please follow this link:  HD Focus Page

  • revision of existing prostheses and tumors involving the entire femur, requiring replacement of both the hip and knee joints
  • fully coupled knee system
  • high degree of modularity and compatibility
  • rotational adjustment in 5° increments
  • reconstruction length can be individually adjusted using extension pieces and the connecting piece
  • 140° CCD angle
  • simplified revision procedures through the use of the connecting piece
  • fixed-bearing PE inserts and mobile-bearing PE inserts with up to 20° of rotation, available in various heights
  • cemented and cementless tibial components
  • cemented and cementless stem options
  • EPORE® Cones and EPORE® metaphyseal components
  • soft tissue reattachment possible using the attachment tube
  • duo mobility options
  • compatible with MUTARS® patella
  • implatan®; TiAl6V4 according to ISO 5832-3 (MUTARS® femoral components, MUTARS® reducer, MUTARS® extension pieces, MUTARS® connecting piece, MUTARS® screws, spacer, offset adapter, cementless GenuX® MK stems)
  • implavit®; CoCrMo according to ISO 5832-4 (ic heads, MUTARS® MOM dist. femur, MUTARS® GenuX® MK tibia, cemented GenuX® MK stems)
  • implavit®; CoCrMo according to ISO 5832-12 (MUTARS® coupling)
  • UHMWPE accordning to ISO 5834-2, implacross® E; cross linked UHMWPE with vitamin E (inserts)
  • TiN coating (optional for MUTARS® femoral component, cemented GenuX® MK stems)
  • TiNbN coating (optional for MUTARS® coupling)
  • implaFix® HA; HA coating according to ISO 13779-2 (optional for cementless GenuX® MK stems)
  • silver coating (optional für MUTARS® extension pieces, MUTARS® connecting piece, MUTARS® reducer, spacer, MUTARS® distal and proximal femur component)
  • EcoFit® 2M cup
  • heads: CoCrMo, ceramic or titanium with TiN, 2M implacross® E heads
  • 2 sizes MUTARS® proximal femur: 50 mm and 70 mm
  • 2 sizes MUTARS® MOM distal femur: 90 mm and 110 mm
  • MUTARS® connecting piece 100 mm
  • 2 sizes MUTARS® reducer: 20 mm and 30 mm
  • 3 options of MUTARS® coupling: 12.5 mm, 15 mm and 17.5 mm
  • 3 heigths of MUTARS® GenuX® MK PE inserts: 12.5 mm, 15 mm and 17.5 mm
  • 5 MUTARS® GenuX® MK tibial components: Gr. 2 – 6
  • MUTARS® GenuX® MK tibia spacer
  • MUTARS® GenuX® MK stems
  • MUTARS® patellar replacement
  • reconstruction length ≥ 280 mm
  • CE Marking

MUTARS® LUMiC®

The MUTARS® LUMiC® is a stem-fixed acetabular component designed for the treatment of tumors, complex and multiple revision cases, as well as very large iliac bone defects. In these challenging situations, it can be used reliably as a hemipelvic replacement.

The MUTARS® LUMiC® is offered as a standard product. As a result, there are no additional waiting times for patients, since it is not a custom-made implant but an immediately available system. To achieve optimal cup orientation and the best possible soft-tissue tension, the implant position can be fine-tuned in 5° increments using a face-serration mechanism, even after stem implantation has already been completed. This allows precise intraoperative adjustment to the individual anatomical situation.

Another key feature is its silver coating. The properties of silver are utilized in the coated components to reduce the risk of infection and increase the longevity of the prosthesis.

  • periacetabular tumours
  • complex or multiple revision procedures
  • massive bone loss associated with Gorham’s disease
  • fractures, pseudarthroses, and osteoarthritis
  • internal hemipelvectomy Type II according to the Enneking classification
  • stem-fixed acetabular cup
  • rotation adjustment in 5° increments
  • cemented and cementless stem options
  • duo mobility options
  • implatan®; TiAl6V4 according to ISO 5832-3 (MUTARS® LUMiC® cups, MUTARS® LUMiC® cementless stems, ic heads titanium)
  • implavit®; CoCrMo according to ISO 5832-4 (MUTARS® LUMiC® cemented stems, MUTARS® LUMiC® 2M inserts 15°, ic heads CoCrMo)
  • UHMWPE in accordance with ISO 5834-2 (EcoFit® 2M head)
  • implacross®; crosslinked UHMWPE (MUTARS® LUMiC® PE inserts)
  • implacross® E; crosslinked UHMWPE with Vitamin E (2M implacross® E head)
  • TiN coating (2M inlay 15° MUTARS® RS cup and LUMiC®)
  • Silver coating (optional for MUTARS® LUMiC® cup ø 60 mm)
  • implaFix® HA; HA coating according to ISO 13779-2 (optional for MUTARS® LUMiC® cementless stems, MUTARS® LUMiC® cup)
  • MUTARS® LUMIC® stems
  • 3 LUMiC® cups: ø 50 mm, ø 54 mm and ø 60 mm
  • implacross® PE inserts 15° neutral 0mm and offset 4mm
  • 2M inserts 15° MUTARS® RS cup and LUMiC®
  • 2M implacross® E head
  • EcoFit® 2M head
  • ic heads 
  • CE Makring
Cement spacer molds and metal augments
cement spacer
CEMPADIC® cement spacer molds
ECOFIT® hip stem
CEMPADIC® acetabulum
cement spacer molds
 
CEMPADIC® acetabulum
cement spacer molds

CEMPADIC® cement spacer molds hip

The two-part CEMPADIC® silicone cement spacer molds allow the surgeon to fabricate a cement spacer intraoperatively whose geometry corresponds to the ECOFIT® cemented hip stem. CEMPADIC® spacer molds allow users to customize their antibiotic treatment.

Reusable up to 25 times

Easy to use, practical application and reusable with a service life of 25 treatment cycles.

CEMPADIC® spacer rods ECOFIT® serve as metal reinforcement for temporary cemented hip stem spacers. These cemented spacers are indicated for septic two-stage prosthesis replacement and serve as antibiotic carriers, space maintainers, and to facilitate passive mobilization of the patient during the course of infection treatment. 

Reinforcing rods with a diameter of 4 mm made of TiAl6V4 are also available.

  • Cempadic® spacer mold EcoFit® stem
    • Alpa-SIL transparent silicone
  • Cempadic® spacer rod EcoFit® stem
    • implatan®; TiAl6V4 acc. to ISO 5832-3
  • 6 sizes femur: 6.25 - 17.5 mm
  • 10 sizes head: 44 - 62 mm
  • 2 sizes spacer rods

Cement
For the preparation of cement spacers, it is recommended to use implabond bone cement with high viscosity. The bone cement can be mixed and applied by hand or using a mixing system and bone cement syringe.

  • CE Marking
EPORE® acetabular spacer  8 mm
EPORE® buttress
EPORE® shim
ic-restrictor acetabulum

Metal augments hip 

Metal augments for the hip include the EPORE® acetabular spacer 8 mm, EPORE® buttress augment, EPORE® shim augment, and the ic-restrictor acetabulum. With the wide range of sizes available, these metal augments for the hip can be used to treat various acetabular defects.

EPORE®

EPORE® is an additively manufactured, highly porous structure made of titanium alloy (TiAl6V4). It is very similar to bone structure, like other porous materials, and probably thus favors the ingrowth of the implant into the bone.

Full Pelvis Solution

When used in combination with the MUTARS® PRS and the MUTARS® PRS reinforcement cage, the EPORE® 8 mm acetabular spacers, EPORE® buttress augments, and EPORE® shim augments become a Full Pelvis Solution.

  • The following indications apply to hip joint replacement using MUTARS® PRS, EPORE® acetabular spacer 8 mm, EPORE® buttress augment, EPORE® shim augment, ic-restrictor acetabulum and MUTARS® PRS reinforcement cage in the acetabular region:
    • non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis
    • post-traumatic osteoarthritis
    • fractures
    • rheumatoid arthritis
       
  • The following additional indication applies to the hip joint replacement with the MUTARS® PRS:
    • large cavitary or segmental acetabular defects (up to type 3a of Paprosky classification)
       
  • The following indication applies to the EPORE® acetabular spacer, EPORE® acetabular spacer 8 mm, EPORE® buttress augment, EPORE® shim augment:
    • acetabular bone defects
       
  • The following indication applies to the ic-restrictor acetabulum:
    • acetabular bone defects
    • presence of a cavitary defect with an intact, load-bearing acetabular rim/ground. (so called contained defect)

Please refer to the Instructions for Use for a full list of indications. 

  • EPORE® acetabular spacer 8 mm
    • removable plugs
    • screws: cancellous bone screw Ø 6.5 mm or Ø 8mm
  • EPORE® buttress augment
    • removable plugs
    • screws: cancellous bone screw Ø 6.5 mm
  • EPORE® shim augment
    • open holes
    • screws: cancellous bone screw Ø 6.5 mm
    • only combinable with EPORE® buttress augment
  • TiAl6V4 with EPORE®
  • EPORE® acetabular spacer 8 mm
    • 26 sizes Ø 46-70 mm
    • hight: 10, 15, 20 and 30 mm* (*30 mm only upon special request)
  • EPORE® buttress augment
    • 4 sizes
      • left posterior /right anterior
      • right posterior / left anterior
      • straight 54 mm
      • straight 58 mm
  • EPORE® shim augment
    • 3 sizes 5°, 10° und 15°
  • ic-restrictor acetabulum
    • 3 sizes 26, 32, 38 mm
  • The metal augments for hip can be combined with certain ic hip cups.
  • For information on compatibility, please refer to the respective surgical techniques.
  • CE Marking