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Uncemented Semi-Constrained Patellofemorotibial Knee Prosthesis Suppliers

 EMAIL INQUIRY to  2 suppliers  
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...
 
Zimmer Gmbh | Address: Sulzer Allee 8, Winterthur CH-8404, Switzerland
FDA Registration: 9613350
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Flexible Depth Gauge (FDA Code: HTJ), Uncemented Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: LWJ), Cemented Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: JDI), Uncemented, Cemented Or Non-Porous Metal/Ceramic/Polymer Semi-Constrained Hip Prosthesis (FDA Code: LZO), ...
Zimmer Gmbh designs and manufactures reconstructive spinal and dental implants, trauma and related orthopedic surgical products. We also offer joint replacement solutions for knee pain and hip pain, a more...
 EMAIL INQUIRY to  2 Uncemented Semi-Constrained Patellofemorotibial Knee Prosthesis suppliers  
FDA Code / Regulation: MBV / 888.3560

A knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components and a retropatellar resurfacing component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027).

Classification. Class II.

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