Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K130673 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version: N/A Product Description... | 2 | 05/31/2024 | CORENTEC CO., LTD |
| LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Ti... | 2 | 05/31/2024 | CORENTEC CO., LTD |
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