Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K091976 |
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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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Phoenix Nail System, intended for use with an intramedullary nail system for alignment, stabilizatio... | 2 | 03/27/2018 | Zimmer Biomet, Inc. |
Various trauma and sports medicine instruments and implants. Rod, fixation, intramedullary and acce... | 2 | 05/26/2016 | Biomet, Inc. |
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