Medical Device Recalls
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61 to 63 of 63 Results
510(K) Number: K070214 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 00,0, l... | 2 | 11/13/2009 | Zimmer Inc. |
Zimmer Gender Solutions Natural-Knee Flex System, Prolong Articular Surface, congruent, Size 00,0, l... | 2 | 11/13/2009 | Zimmer Inc. |
Zimmer Gender Solutions Natural Knee Flex System, Gender Solutions Male, Femoral Component, nonporou... | 2 | 06/26/2009 | Zimmer Inc. |
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