Medical Device Recalls
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1 result found
510(K) Number: K190904 |
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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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| CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO | 2 | 08/16/2023 |
FEI # 3009844603 Conformis, Inc. |
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