Medical Device Recalls
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1 result found
510(K) Number: K071856 |
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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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M/L Taper with Kinectiv® Technology. prosthesis, hip, semi-constrained (metal uncemented acetabular... | 1 | 06/08/2015 | Zimmer, Inc. |
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