Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K992960 |
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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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Atrium ADVANTA VXT Vascular Graft, Part No. 22059, UDI 00650862220599 - Product Usage: intended for ... | 2 | 09/29/2021 | Atrium Medical Corporation |
Advanta VXT Vascular Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmenta... | 2 | 09/30/2013 | Atrium Medical Corporation |
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