Hip
Product Groups
Select an anatomical region to view the corresponding products.
General additional products
ic cement restrictor resorbable and intramedullary plug
The ic cement restrictor resorbable and the intramedullary plug are used for the obturation of the medullary cavity before inserting bone cement. The intramedullary plug is designed to be inserted into the medullary canal of a bone before bone cement is applied. It is intended for the prevention of cement progression in the diaphysis.
Intended use:
- ic cement restrictor resorbable
- The ic cement restrictor resorbable cement restrictor is a diaphyseal plug intended to occlude the medullary cavity before the introduction of acrylic cement during hip arthroplasty surgeries.
- The ic cement restrictor resorbable cement restrictor is a diaphyseal plug intended to occlude the medullary cavity before the introduction of acrylic cement during hip arthroplasty surgeries.
- intramedullary plug
- The intramedullary plug (non-bioabsorbable) is designed to be inserted into the medullary canal of a bone before bone cement is applied. It is intended for the prevention of cement progression in the diaphysis.
- ic cement restrictor resorbable:
- The ic cement restrictor resorbable is an implantable device, intended to be totally dissolved and metabolised by the organism within a time lag of 1 to 15 days. This period may vary depending on the physiological condition of the patient.
- ic cement restrictor resorbable
- gelatin (porcine-based)
- glycerin
- water
- methylparahydroxybenzoate
- intramedullary plug
- UHMWPE acc. to ISO 5834-2, X-ray wire TiAl6V4 acc. to ISO 5832-3
- ic cement restrictor resorbable
- 6 sizes Ø 8 - 18 mm
- intramedullary plug
- 2 sizes
- small (medullary cavity Ø 9-13 mm)
- large (medullary cavity Ø ≥ 14 mm)
The Instructions for Use and the surgical technique for the combined systems or implants must also be followed.
- CE Marking
Surgical saw blades
Flexoral strength and cutting precision significantly influence the surgical outcome!
The teeth are diamond-cut and are arranged in a double row. The continuous blade thickness from the holder to the cutting edge enables atraumatic cuts and reduces metal abrasion against the saw guide. Due to the use of special stainless steel, there is no deviation of the saw blade from the cutting direction even with deep cuts (tibia plateau cut). The diamond cut design also minimizes the otherwise known rapid blunt of the saw blade, drastically reducing the risk of thermal necrosis.
In combination with the instruments developed by implantcast, the saw blades enable precise and reliable preparation. The products are compatible with the following machines: Aesculap 3Ti, Stryker System 2000 / 4 / 5 / 6, Synthes, and Zimmer/Hall Versipower plus.
In no other operation is the demand on the saw blade higher than within endoprosthetics. This graphic shows how the measurements were determined.
Stainless Steel
- Aesculap
- Aesculap thickness: 1,37 mm, width: 13 mm, length: 105 mm
- Aesculap thickness: 1,37 mm, width: 17 mm, length: 105 mm
- Aesculap thickness: 1,37 mm, width: 25 mm, length: 105 mm
- Aesculap 3Ti
- Synthes thickness: 1,37 mm, width: 13 mm, length: 105 mm
- Synthes thickness: 1,37 mm, width: 17 mm, length: 105 mm
- Synthes thickness: 1,37 mm, width: 25 mm, length: 105 mm
- Stryker System 2000/4/5/6
- Stryker 2000 / 4 / 5 / 6 thickness: 1,37 mm, width: 13 mm, length: 105 mm
- Stryker 2000 / 4 / 5 / 6 thickness: 1,37 mm, width: 17 mm, length: 105 mm
- Stryker 2000 / 4 / 5 / 6 thickness: 1,37 mm, width: 25 mm, length: 105 mm
- Synthes
- Synthes thickness: 1,37 mm, width: 13 mm, length: 105 mm
- Synthes thickness: 1,37 mm, width: 17 mm, length: 105 mm
- Synthes thickness: 1,37 mm, width: 25 mm, length: 105 mm
- Zimmer/Hall Versipower plus
- Zimmer/Hall Versipower plus thickness: 1,37 mm, width: 13 mm, length: 105 mm
- Zimmer/Hall Versipower plus thickness: 1,37 mm, width: 17 mm, length: 105 mm
- Zimmer/Hall Versipower plus thickness: 1,37 mm, width: 25 mm, length: 105 mm
- Divserse
- Aesculap/Synthes/How thickness: 0,7 mm, width: 10 mm
- Linvatec/Micro thickness: 0,4mm, width: 6 mm, length: 34 mm
MUTARS® attachment tube
The MUTARS® attachment tube has been developed to enable the secure reattachment of muscle and tendon tissue as well as capsular and ligamentous structures to modular endoprostheses. Its mesh-like structure supports the biological integration of soft tissue and contributes to the restoration of stable anatomical conditions. Particularly in complex reconstructions, the attachment tube facilitates improved soft tissue fixation and supports postoperative joint stability.
The MUTARS® attachment tube is primarily used in major reconstructive procedures following tumor resections or complex revision surgeries where secure reattachment of soft tissue structures is required. Typical applications include reconstructions of the proximal humerus for reattachment of the rotator cuff, the proximal femur for reattachment of the joint capsule and surrounding musculature, and the proximal tibia for reattachment of muscle flaps (e.g. the gastrocnemius muscle), the extensor mechanism, and the patellar tendon.
- secure fixation of muscle, tendon, capsular, and ligamentous tissue to the endoprosthesis
- may reduce the risk of dislocation, particularly in proximal humeral and proximal femoral reconstructions
- Polyethyleneterephthalate (PET)
- length: 300 mm
- diameter: 35 mm or 55 mm
- CE Marking
ic-Cerclage
ic-cerclages are intended for the fixation and reduction of bone fragments (seamless and non-absorbable) as well as for additional fixation and reduction in conjunction with bone plate and screw systems.
The 8 mm ic-cerclage is made of pure titanium and is used to treat bone fractures of large hollow bones and is available in two versions (matt or roughly blasted on bone side). It is adjusted and clamped intraoperatively with a special cerclage tensioner on length or rather on bone range so that the compression is exerted on the bone. The tape will also be applied prophylactic in prosthetic implants to prevent potential occuring stem scissures and blasts.
- ic-cerclage
- width: 8 mm
- surface matt blasted on both sides
- ic-cerclage band titanium 2R
- width: 8 mm
- surface roughly blasted on the bone side
- ic-titanium cerclage wire
- Ø 1,4 mm
- length: 50 cm / 5 m
- pure titanium acc. to ISO 5832-2 Grade 1
- ic-cerclage: 1 size
- ic-cerclage band titanium 2R: 1 size
- ic-titanium cerclage wire: 2 sizes
- CE Marking
CERASORB®
Synthetic bone regeneration materials are used in orthopaedics and traumatology to treat bone defects caused by trauma or disease. The CERASORB® product family comprises fully resorbable bone regeneration materials made from high-purity, phase-pure β-tricalcium phosphate (β-TCP). The portfolio includes CERASORB® M granules, CERASORB® Foam and CERASORB® CPC injectable bone cement, providing user-friendly solutions for a range of clinical requirements in bone regeneration.
Thanks to their osteoconductive properties, CERASORB® products support the formation of new bone within the defect site. During the healing process, the material is completely remodelled and replaced by the patient’s own bone. In accordance with the instructions for use, CERASORB® Foam may also be used as a local antibiotic carrier
Depending on the product variant, the CERASORB® product family is suitable for applications including:
- foot and ankle
- wrist
- shoulder Fractures
- joint revisions
- oncological defects
- traumatology
- spine
- CERASORB® M
- resorbable, phase-pure β-tricalcium phosphate
- interconnected multiporosity with micro-, meso-, and macropores (5–500 μm)
- total porosity of approximately 65%
- polygonal granule structure promotes interlocking within the defect site
- complete resorption without material residue
- CERASORB® Foam
- highly porous composite of porcine collagen and phase-pure β-tricalcium phosphate
- available as Mouldable Foam and Flexible Foam Strip
- rapid hydration
- mouldable or elastic, depending on the product variant
- can be individually loaded with suitable antibiotics
- completely remodelled into the patient’s own bone
- CERASORB® CPC
- injectable, self-setting biomineral bone cement
- ready to use with no mixing required
- self-setting in an aqueous environment
- high cohesion and compressive strength
- resorbed and replaced by the patient’s own bone
- CERASORB® M
- resorbable, phase-pure β-tricalcium phosphate with interconnected multiporosity
- resorbable, phase-pure β-tricalcium phosphate with interconnected multiporosity
- CERASORB® Foam
- Highly porous composite of phase-pure β-tricalcium phosphate and a porcine collagen matrix.
- The collagen matrix stabilises the β-TCP granules and provides high volume stability after the collagen has degraded.
- CERASORB® CPC
- Biomineral calcium phosphate cement consisting of calcium phosphate powder and a biocompatible oil-phase solution.
- The self-setting process produces microcrystalline, calcium-deficient hydroxyapatite.
- CERASORB® M
- resorbable granules available in various granule sizes and pack sizes
- resorbable granules available in various granule sizes and pack sizes
- CERASORB® Foam
- mouldable Foam (low density)
- flexible Foam Strip (high density)
- flexible Foam XL for larger defect volumes
- CERASORB® CPC
- injectable bone cement available in 6 ml and 12 ml
implabond bone cement
implabond bone cements with gentamicin are intended for the fixation of prosthetic components within the medullary cavity of bones during joint replacement surgery.
implabond bone cements are indicated for use in cemented arthroplasty procedures.
- implabond 1G is indicated for primary (shoulder, hip, knee) and revision (knee) surgeries.
- implabond 3G is indicated for primary (hip) and revision (hip, knee) surgeries.
implabond bone cements enable the secure fixation of prosthetic implants and provide effective antibiotic protection.
- powder
- polymethylmethacrylate
- benzoyl peroxide
- barium sulphate
- gentamicin sulphate
- liquid
- methylmethacrylate
- butylmethacrylate
- N-N dimethyl–p-toluidine
- hydroquinone
- implabond 1G
- bone cement 40 g high viscosity
- implabond 3G
- bone cement 40 g low viscosity
- CE Marking









