Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K970031 |
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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 Tibial Broach P/N 801-01-013 Foundation Tibial Broach to be used in conjunction with... | 2 | 12/02/2011 | Encore Medical, Lp |
FOUNDATION KNEE SYSTEM Tibial Fixed Impactor, Revision A and B; Catalog #801-01-449; distributed by ... | 2 | 09/29/2008 | Encore Medical, Lp |
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