Medical Device Recalls
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1 result found
510(K) Number: K153657 |
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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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XP-XP Tibial Tray - Interlok 59 mm Item # 195750 | 2 | 09/12/2019 | Zimmer Biomet, Inc. |
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