Medical Device Recalls
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1 result found
510(K) Number: K923807 |
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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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P.F.C.® Modular Knee System Modular Plus Tibial Wedge 10® HEMI x 8.5MM HEIGHT Product Code: 86-01... | 3 | 08/24/2004 | Depuy Orthopaedics, Inc. |
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