Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K142579 |
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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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PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL, Item Nos. 00234801303 00234801304 00234801306 002... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
Periarticular Plates - Tibial, Item Nos. 00234700304 00234700306 00234700308 00234700310 0023470... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
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