Medical Device Recalls
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1 result found
510(K) Number: K022672 |
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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 R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN058K NN070... | 2 | 03/13/2020 | Aesculap Implant Systems LLC |
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