Medical Device Recalls
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1 result found
510(K) Number: K110449 |
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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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Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or s... | 2 | 02/09/2016 | Biomet France SARL |
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