Medical Device Recalls
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1 result found
510(K) Number: K071220 |
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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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AS COLUMBUS CR/PS TIB.PLAT.CEMENTED,Knee implant components, various sizes, model nos. NN058Z NN0... | 2 | 03/13/2020 | Aesculap Implant Systems LLC |
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