Medical Device Recalls
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1 result found
510(K) Number: K983153 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Natural-Knee¿ II Posterior Stabilized (P.S.) Condylar Tibial Inserts: N-K II CONS PS TIB INS SZ N-... | 2 | 03/20/2014 |
FEI # 1000220733 Zimmer, Inc. |
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