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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K992958
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ADVANTA VXT, 4-7X45, 2GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
ADVANTA VXT, 4-6X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
ADVANTA VXT, 4-7X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
ADVANTA VXT, 4-7X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft 2 06/04/2024 FEI # 3011175548
Atrium Medical Corporation
Advanta VXT Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and... 2 09/30/2013 FEI # 3011175548
Atrium Medical Corporation
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