Medical Device Recalls
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1 result found
510(K) Number: K082615 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix... | 2 | 09/08/2023 |
FEI # 1000477302 Medtronic Sofamor Danek USA Inc |
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