Product Wiki · Recalls · U.S. FDA — Device Enforcement
U.S. FDA — Device Enforcement · United States · 2016-01-11 · Class II
As described by U.S. FDA — Device Enforcement: NexGen LPS-FLEX Option Femoral NexGen LPS-FLEX Precoat Femoral prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer various sizes Product Usage "" This device is indicated for patients with severe knee pain and disability due to: Rheumatoid arthritis, osteoa
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