Medical Device Recalls
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1 result found
510(K) Number: K060763 |
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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 Part Numbers 79-43903 (3cc), 79-43905 (5cc), 79-43910 (10 cc), 79-43915 (15cc), 397003 (3cc... | 2 | 08/26/2013 | Stryker Craniomaxillofacial Division |
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