Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K042093 |
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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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Knee Products: US154709 Knees Vanguard M Partial Knee System MonoBlock Tibial Tray, Right Medial/Le... | 2 | 05/28/2020 | Biomet, Inc. |
Vanguard M Unicondylar Tibial Trial For use during knee joint replacement. | 2 | 06/15/2015 | Biomet, Inc. |
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