Medical Device Recalls
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1 result found
510(K) Number: K954800 |
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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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CoCr Femoral Head - indicated for hip arthroplasty for noncemented use in skeletally mature invididu... | 2 | 02/20/2015 | Zimmer Gmbh |
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