Medical Device Recalls
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1 result found
510(K) Number: K050222 |
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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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| Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. The product ... | 2 | 04/22/2024 | Biomet, Inc. |
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