Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K090596 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Zimmer Natural Nail System, Antegrade Femoral Targeting Guide Handle, tall, nonsterile, Zimmer, Wars... | 2 | 11/24/2009 | Zimmer Inc. |
Zimmer Natural Nail System, Antegrade Femoral interlock Module, tall, nonsterile, Zimmer, Warsaw, IN... | 2 | 11/24/2009 | Zimmer Inc. |
Zimmer Natural Nail System, Connecting Knob, nonsterile, Zimmer, Warsaw, IN; REF 00-2490-000-11. ... | 2 | 11/24/2009 | Zimmer Inc. |
Zimmer Natural Nail System, Tibial Module, nonsterile, Zimmer, Warsaw, IN; REF 00-2490-005-04. Th... | 2 | 11/24/2009 | Zimmer Inc. |
Zimmer Natural Nail System, Tibial Targeting Guide Handle, small, nonsterile, Zimmer, Warsaw, IN; RE... | 2 | 11/24/2009 | Zimmer Inc. |
Zimmer Natural Nail System, Tibial Targeting Guide Handle, tall, nonsterile, Zimmer, Warsaw, IN; REF... | 2 | 11/24/2009 | Zimmer Inc. |
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