Medical Device Recalls
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1 result found
510(K) Number: K133518 |
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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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MaxAn 4.0mm and 4.5mm fixed screws, used in the MaxAn Anterior Cervical Plate System. The MaxAn Ante... | 2 | 11/03/2015 | Biomet Spine, LLC |
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