Medical Device Recalls
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1 result found
510(K) Number: K974685 |
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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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| Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixati... | 2 | 01/15/2020 |
FEI # 3003070421 Howmedica Osteonics Corp. |
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