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Porous Uncemented Metal/Ceramic/Polymer + Additive Cemented Semi-Constrained Hip Suppliers

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Biomet, Inc | Address: PO Box 587, Warsaw, Indiana 46581-0587, USA USA
www.biomet.com/orthopedics | Send Inquiry | Phone: +1-(574)-267-6639
FDA Registration: 1825034  Year Established: 1977  Annual Revenues: > USD 1 Billion  Employee Count: ~20  Quality: ISO 9001, CE Certified
Products: Drills, Drills Accessories, High Speed Orthopedic Drills, Surgical Drills, Orbital Procedures, Bone Drills, Orthopedics, High Speed Drills System, ...
Biomet, Inc designs and manufactures products for hip replacement, knee replacement, shoulder replacement, elbow replacement & other small joint replacements. We are an ISO 9001 CE certified company. more...
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 EMAIL INQUIRY to  1 Porous Uncemented Metal/Ceramic/Polymer + Additive Cemented Semi-Constrained Hip suppliers  
FDA Code / Regulation: OQI / 888.3353

A hip joint metal/ceramic/polymer semi-constrained cemented or nonporous uncemented prosthesis is a device intended to be implanted to replace a hip joint. This device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. The two-part femoral component consists of a femoral stem made of alloys to be fixed in the intramedullary canal of the femur by impaction with or without use of bone cement. The proximal end of the femoral stem is tapered with a surface that ensures positive locking with the spherical ceramic (aluminium oxide, A1203) head of the femoral component. The acetabular component is made of ultra-high molecular weight polyethylene or ultra-high molecular weight polyethylene reinforced with nonporous metal alloys, and used with or without bone cement.

Classification. Class II.

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