Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K972863 |
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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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DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-609 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-711 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-709 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-611 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
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