Stent, Vena Cava
FDA product code QTL · 2 devices · 2 reports · 0 devices named in recalls
- GORE® VIABAHN® FORTEGRA Venous Stent VNS181002AW. L. Gore & Associates, Inc. · Stent, Vena Cava1 report
- GORE® VIABAHN® FORTEGRA Venous Stent VNS141002AW. L. Gore & Associates, Inc. · Stent, Vena Cava1 report