Medical Device Recalls
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1 result found
510(K) Number: K110836 |
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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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| CLS Brevius Stem Kinectiv, hip prosthesis, various sizes. Item Nos. 0100296050 0100296060 01002960... | 2 | 11/07/2019 |
FEI # 1000220733 Zimmer Biomet, Inc. |
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