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Semi-Constrained Patellofemoral Knee Prosthesis Suppliers

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Global Manufacturing Technology Pty Ltd. | Address: 8 Resolution Drive, Unanderra, Wollongong, New South Wales 2526, Australia
Phone: +61-(2)-427-24493
FDA Registration: 3004537778
Products: Semi-Constrained Femorotibial Knee Prosthesis (FDA Code: HRY), Semi-Constrained Patellofemoral Knee Prosthesis (FDA Code: KRR), ...
Global Manufacturing Technology Pty Ltd. supplies a range of knee prosthesis. Our products include semi-constrained femorotibial knee prosthesis and semi-constrained parallelogram knee prosthesis. more...
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  21 to 21 of 21 Semi-Constrained Patellofemoral Knee Prosthesis suppliers  Page: << Previous 20 Results 1 [2]
FDA Code / Regulation: KRR / 888.3540

A knee joint patellofemoral polymer/metal semi-constrained cemented prosthesis is a two-part device intended to be implanted to replace part of a knee joint in the treatment of primary patellofemoral arthritis or chondromalacia. 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 a component made of alloys, such as cobalt-chromium-molybdenum or austenitic steel, for resurfacing the intercondylar groove (femoral sulcus) on the anterior aspect of the distal femur, and a patellar component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those devices intended for use with bone cement (888.3027). The patellar component is designed to be implanted only with its femoral component.

Classification. Class II. The special controls for this device are:

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