Medical Device Recalls
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1 result found
510(K) Number: K904208 |
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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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| Kinemax Stem Extenders, 80 mm, Product Usage: Kinemax Cemented Stem Extenders are modular compone... | 2 | 05/14/2015 |
FEI # 3003070421 Stryker Howmedica Osteonics Corp. |
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