Medical Device Recalls
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1 result found
510(K) Number: K932246 |
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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, Patella Trial, 26 mm, part number 802-01-019, Lot number 53944551 | 2 | 04/07/2010 | Encore Medical, Lp |
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