Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121771 |
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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 Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Bra... | 2 | 06/07/2016 | Zimmer Biomet, Inc. |
Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis, Knee, Patello/Femorotibial, Sem... | 2 | 03/12/2015 | Zimmer, Inc. |
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