Medical Device Recalls
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1 result found
510(K) Number: K974728 |
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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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Metasul Femoral Head - indicated for total hip arthroplasty for treatment of patient conditions of ... | 2 | 02/20/2015 | Zimmer Gmbh |
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