Medical Device Recalls
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1 result found
510(K) Number: K930156 |
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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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Short Barrel Sideplate, Omega + 140 degrees, 4 slots; The Omega Plus Compression Screw system consis... | 2 | 09/16/2008 | Stryker Howmedica Osteonics Corp. |
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