Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K030978 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Scorpio NRG Posterior Stabilized Femoral, # 5 Left; Stryker Orthopaedics, 325 Corporate Drive, Mahw... | 2 | 12/01/2009 | Stryker Howmedica Osteonics Corp. |
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