Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K041170 |
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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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Primary Secur-fit Plus Max Hip Stem These devices are modular components of a total hip system. T... | 2 | 01/26/2009 | Stryker Howmedica Osteonics Corp. |
Secur-Fit Max Hip Stem These devices are modular components of a total hip system. These femoral ... | 2 | 01/26/2009 | Stryker Howmedica Osteonics Corp. |
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