Medical Device Recalls
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1 result found
510(K) Number: K000080 |
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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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Stryker 1) Asnis III Cannulated Screw REF 604640 4.0x40mm TL 13.5mm 2) Asnis III Cannulated Sc... | 2 | 08/27/2013 | Stryker Howmedica Osteonics Corp. |
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