Medical Device Recalls
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1 result found
510(K) Number: K033995 |
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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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Synthes 3.5 MM LCP(R) Distal Humerus System The Synthes 3.5 MM LCP Distal Humerus System is inten... | 2 | 09/25/2013 | Synthes USA HQ, Inc. |
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