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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K031572
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Xl por st 24.0x220mm, bowed, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee... 2 03/20/2017 Zimmer Biomet, Inc.
Xl por st 25.5x220mm, bowed\, bowed, Sterile, Rod, fixation, intramedullary and accessories- Speci... 2 03/20/2017 Zimmer Biomet, Inc.
ZMR Over the Junction Instruments for Revision, utilized for the following ZMR devices: Porous Stem,... 2 12/01/2011 Zimmer Inc.
ZMR Porous Revision Hip Prosthesis Surgical Technique, utilized for the following ZMR devices: Porou... 2 12/01/2011 Zimmer Inc.
Zimmer ZMR Hip System Instructions for Use, utilized for the following ZMR devices: Porous Stem,Nitr... 2 12/01/2011 Zimmer Inc.
ZMR Crossover Instrumentation, utilized for the following ZMR devices: Porous Stem,Nitrited Porous R... 2 12/01/2011 Zimmer Inc.
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