Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K122765 |
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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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Persona Cemented Tibial SZ PLT Size H Left, Item Number 42539908301 For use during orthopaedic s... | 2 | 05/11/2018 | Zimmer Biomet, Inc. |
PERSONA® THE PERSONALIZED KNEE SYSTEM "PSN TIB STM 5 DEG SZ D R" indicated for patients with severe ... | 2 | 03/27/2018 | Zimmer Biomet, Inc. |
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