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U.S. Department of Health and Human Services

Medical Device Recalls

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31 to 40 of 83 Results
510(K) Number: K933785
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Product Description
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Recall
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FDA Recall
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00-5970-020-20 NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular C... 2 05/14/2012 Zimmer Inc.
90-5970-020-09, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.
90-5970-020-10, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) 10 MM Height , Use With Pl... 2 05/14/2012 Zimmer Inc.
90-5970-020-12, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.
90-5970-020-14, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.
90-5970-020-17, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.
90-5970-020-20, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.
00-5972-020-09, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.
00-5972-020-10, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.
00-5972-020-12, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.
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