Medical Device Recalls
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1 result found
510(K) Number: K130703 |
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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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Vivorte Trabexus EB 10 cc Bone Void Filler -Fill bone and/or defect in skeletal system Model Numbe... | 2 | 07/07/2021 | Vivorte, Inc. |
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