Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K923277 |
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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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FOUNDATION KNEE SYSTEM Tibial Fixed Impactor, Revision A and B; Catalog #801-01-449; distributed by ... | 2 | 09/29/2008 | Encore Medical, Lp |
Size 6 right Foundation Total Knee System (Catalog #324-01-106) knee joint replacement. | 2 | 12/29/2005 | Encore Medical, Lp |
Foundation Knee System, Tibia-Nonporous, Size 6, Right, sterile. Manufactured by Encore Orthopeadic... | 3 | 07/20/2004 | Encore Medical, LP |
Foundation Knee System, non-porous Femur Size 8, Right | 2 | 07/30/2003 | Encore Medical, LP |
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