GORE® TAG® Conformable Thoracic Stent Graft with ACTIVE CONTROL System Case Studies
Sukgu Han, M.D. shares an example of optimal TEVAR positioning in a Type B dissection*
Case video: Growing TAA with short angulated landing zone*
Case video: Saccular aneurysm with suspicion of contained rupture*
Case video: Two examples of device placement optimization*
Polytrauma Emergency Implantation into the Aortic Arch*
* These results are individual observations of the physician, and not representative for all uses of the device
Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly
INDICATIONS FOR USE IN THE U.S.: The GORE® TAG® Conformable Thoracic Stent Graft is intended for endovascular repair of all lesions of the descending thoracic aorta, including: isolated lesions in patients who have appropriate anatomy, including: adequate iliac/femoral access, aortic inner diameter in the range of 16-42 mm, ≥ 20 mm non-aneurysmal aorta proximal and distal to the lesion; Type B dissections in patients who have appropriate anatomy, including: adequate iliac/femoral access, ≥ 20 mm landing zone proximal to the primary entry tear; proximal extent of the landing zone must not be dissected, diameter at proximal extent of proximal landing zone in the range of 16-42 mm.
CONTRAINDICATIONS: Patients with known sensitivities or allergies to the device materials; patients who have a condition that threatens to infect the graft.