Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K003294 |
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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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| Lateral Troch Plate Full Crimp - 254mm, model # 350838 | 2 | 12/29/2017 |
FEI # 1825034 Zimmer Biomet, Inc. |
| Lateral Troch Plate Full Crimp - 254mm, model # 350837 | 2 | 12/29/2017 |
FEI # 1825034 Zimmer Biomet, Inc. |
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