Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K021026 |
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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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S2 System, Locking Screw Fully Threaded | 2 | 11/18/2005 | Stryker Howmedica Osteonics Corp. |
S2 System, Locking Screw Partially Threaded | 2 | 11/18/2005 | Stryker Howmedica Osteonics Corp. |
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