Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K884398 |
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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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| SERIES II TIBIAL BEAR INSERT-Intended for knee replacement Part Number: 3052-0524 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
| SERIES II TIBIAL BEAR INSERT-Intended for knee replacement Part Number: 3052-0515 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
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