Medical Device Recalls
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1 result found
510(K) Number: K143576 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Exactech Single Barrel Drill Guides The Single Barrel Drill Guide is a nonpowered hand-held device ... | 2 | 07/14/2015 | Exactech, Inc. |
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