Medical Device Recalls
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1 result found
510(K) Number: K121627 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicat... | 2 | 01/04/2017 |
FEI # 1020279 Smith & Nephew, Inc. |
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