Medical Device Recalls
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1 result found
510(K) Number: K943540 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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REF 5100-088, TPS Micro Driver, For Use with Stryker Total Performance System Caution Federal La... | 2 | 10/28/2013 | Stryker Instruments Div. of Stryker Corporation |
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