Medical Device Recalls
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1 result found
510(K) Number: K830121 |
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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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I/B II KNEE DOMED PATELLA, I/B II KNEE FLUTED ROD (1 and 2), MGII KNEE 10MM PATELLA (2,3 and 4), MGI... | 2 | 02/20/2014 | Zimmer, Inc. |
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