Medical Device Recalls
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1 result found
510(K) Number: K041911 |
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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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| Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur ... | 2 | 11/27/2013 |
FEI # 3005180112 Synthes USA HQ, Inc. |
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