News

Endurant IIs, stent graft system, abdominal aortic aneurysm, AAA

Medtronic Inc. announced the launch in Europe and the United States of the Endurant IIs AAA stent graft, which received CE mark and U.S. Food and Drug Administration approval to be used in...

Oxford clinical study, American Heart Association, abdominal aortic aneurism

Oxford University researchers presented data that reveal the extent to which smoking causes silent but deadly damage to health at the annual scientific meeting of the American Heart Association (...

Aortic Aneurysm, stent graft, Gore Excluder

Pierre Galvagni Silveira, M.D., Ph.D. enrolled the first two patients in the Gore Thoracoabdominal Aortic Aneurysm Clinical Study. This initial feasibility study of the Gore Excluder...

VIVA Physicians, a not-for-profit organization in the field of vascular medicine and intervention, announced late-breaking clinical trial results VIVA 14, an annual multidisciplinary...

Lombard Medical Inc., a medical device company focused on endovascular aneurysm repair (EVAR) of abdominal aortic aneurysms (AAA), today announced that its lead product, Aorfix, an...

W.L. Gore FDA Approval Gore Viabahn Endoprosthesis

W. L. Gore & Associates Inc. announced that the U.S. Food and Drug Administration (FDA) has approved the Gore Viabahn Endoprosthesis for interventional treatment of in-stent restenosis in the...

September 15, 2014 — A new minimally invasive surgery involving a stent graft made from a 3-D image of the patient’s anatomy could eliminate the need for open surgery for some patients suffering...

MicroVention LVIS Stent FDA Clearance July 2014

The U.S, Food and Drug Administration (FDA) has cleared MicroVention Inc.’s Low-Profile Visualized Intraluminal Support Device (LVIS and LVIS Jr.), which is a stent and delivery system...

July 15 2014 — Researchers at the University of California, San Diego School of Medicine have documented the safety benefits of aortic stent grafts inserted during minimally invasive surgery to...

Pulsar Vascular announced it received U.S. Food and Drug Administration (FDA) investigative device exemption (IDE) approval for the PulseRider, a minimally invasive aneurysm neck reconstruction...

Medtronic Valiant Captiva Thoracic Stent Graft Total Support Catheter US Market

Continuing to expand its portfolio of endovascular solutions, Medtronic Inc. announced that two recently U.S. Food and Drug Administration (FDA) approved devices will be featured at the Society...

Simbionix ANGIO Mentor Flex Endovascular Training

As more endovascular medical programs adapt simulation as an essential part of their training curriculum, there is a constant and consistent need for updated simulation solutions. Simbionix is...

Gore Tag Thoracic Branch Endoprosthesis LSA Feasibility Study Clinical Trial

W. L. Gore & Associates (Gore) announced that Himanshu Patel, M.D. and David Williams, M.D. at The University of Michigan enrolled the first patient in the Gore TAG Thoracic Branch...

Gore Excluder AAA Stent Graft

W. L. Gore & Associates’ Gore Excluder Iliac Branch Endoprosthesis is a complete, fully engineered system intended for endovascular treatment of common iliac artery aneurysms or aortoiliac...

Medtronic Valiant Captivia Thoracic Stent Graft System Aneurism Repair AAA TAA

The U.S. Food and Drug Administration (FDA) Medtronic Inc.’s Valiant Captivia Thoracic Stent Graft System to treat type B aortic dissections. Supported by the results of the U.S. Medtronic...

Gore AAAneurysm Outreach Abdominal Aortic Aneurysm AAA Stent Graphs

W. L. Gore & Associates Inc. (Gore) and AAAneurysm Outreach have partnered to raise awareness and drive screening of individuals at-risk of ...

Gore Viabahn Endoprosthesis Heparin Bioactive Surface Stent Grafts Aneurism

January 28, 2014 — The U.S. Food and Drug Administration (FDA) approved W. L. Gore & Associates’ 25 cm Gore Viabahn Endoprosthesis with Heparin Bioactive Surface for the treatment of...

aneurism repair stent graft endologix nellix endovascular evas

Endologix Inc. announced that it has received Investigational Device Exemption (IDE) approval from the U.S. Food and Drug Administration (FDA) to begin a clinical trial to evaluate the safety and...

simulators cath lab aneurism repair TCT 2013 simbionix procedure rehearsal

Simbionix, a provider of innovative training solutions, announced the initiation of the REHEARSAAAL study which evaluates the clinical benefits of preoperative patient specific simulation using...

The U.S. Food and Drug Administration (FDA) announced a final rule for the unique device identification system (UDI) that, once implemented, will provide a consistent way to identify...