Medical Device Recalls
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1 result found
510(K) Number: K111746 |
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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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Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic implants for Proximal Humera... | 2 | 03/23/2018 | Biomet, Inc. |
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