Medical Device Recalls
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1 result found
510(K) Number: K121589 |
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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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1.5mm System, Cranio-maxillofacial Bone Screws 1.5 x 4mm HT SD X-DR Screw, Bone Screw | 2 | 02/16/2017 | Zimmer Biomet, Inc. |
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