Medical Device Recalls
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1 result found
510(K) Number: K053390 |
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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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COLUMBUS CRA/PSA TIB.PLAT.CEMENTED, Knee implant components, various sizes, model nos. NN469K NN47... | 2 | 03/13/2020 | Aesculap Implant Systems LLC |
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