Medical Device Recalls
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1 result found
510(K) Number: K062915 |
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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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VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excl... | 2 | 01/08/2021 | Baxter Healthcare Corporation |
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