Medical Device Recalls
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1 result found
510(K) Number: K132624 |
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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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Trial Cutting Guide for Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee System,... | 2 | 04/09/2021 | Howmedica Osteonics Corp. |
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