GORE MEDICAL RECEIVES BREAKTHROUGH DEVICE DESIGNATION FOR THE GORE® EXCLUDER® THORACOABDOMINAL BRANCH ENDOPROSTHESIS
CAUTION: Investigational device. Limited by United States law to investigational use.
Apr 12, 2022
CAUTION: Investigational device. Limited by United States law to investigational use.
Apr 12, 2022
Multi-Center Study to Assess Feasibility of Gore Device to Treat Historically Challenging Patient Population
Completion of follow -up paves way for REDUCE Clinical Study data submission to FDA for PFO indication
108 patient trial to add evidence for treatment of in-stent restenosis using the GORE® VIABAHN® Endoprosthesis
Decision comes after two-year effort to improve the alignment of payment with cost of treatment for abdominal aortic aneurysms
New three-layer hybrid biomaterial, ideal for TAR procedures, offering permanent strength and rapid tissue generation for single-stage repairs
Designation recognizes products that bring improvements to the healthcare industry
New sheath provides exceptional access to challenging anatomies and branch vessels
GORE® Ascending Stent Graft, an investigational device, is an off-the-shelf endovascular solution designed to treat life-threatening Type A dissections of the ascending aorta