Medical Device Recalls
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1 result found
510(K) Number: K031744 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Omnifit HFX Hip Stem These devices are modular components of a total hip system. These femoral stem... | 2 | 01/26/2009 | Stryker Howmedica Osteonics Corp. |
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