Medical Device Recalls
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51 to 51 of 51 Results
510(K) Number: K033272 |
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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| Depuy P.F.C. SIGMA curved insert; polyethylene tibial insert , Sz 2.5, 8 mm; Ref 1581-12-008. | 2 | 08/12/2005 | Depuy Orthopaedics, Inc. |
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