Medical Device Recalls
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1 result found
510(K) Number: K081860 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Segmental vss bowed 19x190mm, Sterile, Hip joint, metal/ceramic/polymer, semi-constrained, cemente... | 2 | 03/20/2017 | Zimmer Biomet, Inc. |
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