Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K113060 |
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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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Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arthropla... | 2 | 11/02/2023 | Corin Ltd |
Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty | 2 | 11/02/2023 | Corin Ltd |
Unity Total Knee System. Used for knee prosthesis in total knee replacement | 2 | 11/21/2022 | Corin Ltd |
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