Bolton Medical, a medical device manufacturer, has initiated its Phase II US clinical trial to study the safety and effectiveness of the Treovance abdominal stent-graft with Navitel delivery system. The first two cases were performed on ...
Medtronic's Valiant 'Mona LSA' branch thoracic stent graft system demonstrated proof of concept in a first-in-human study being conducted under the US Food and Drug Administration (FDA)'s ‘Innovation Pathway’ early feasibility ...
Tags: stent graft system, Medicine
Medical technology company Lombard Medical Technologies successfully treated the first US patients with Aorfix, its flexible stent graft for the endovascular repair of abdominal aortic aneurysms (AAAs). Meriter Hospital vascular surgeon ...
Tags: Aortic Stent Graft
US medical device company TriVascular has commenced the US Post-Approval Study (PAS) of the Ovation Prime Abdominal Stent Graft System for the treatment of abdominal aortic aneurysms (AAA). The Ovation System and the Ovation Prime System ...
Tags: TriVascular, medical device
The European Union (EU) has granted CE mark certification to Medtronic's Sentrant Introducer Sheath for the endovascular repair of aortic aneurysms. Designed for use with the company's Endurant II AAA and Valiant Captivia Stent Graft ...
Tags: aortic aneurysms, Medtronic, Sentrant Introducer Sheath
Aptus Endosystems has received CE mark approval from the European Union for its thoracic-length Heli-FX system for thoracic aortic aneurysms (TAA) treatment. Featuring a longer delivery device with additional tip configurations, the ...
Tags: Heli-FX System, Medicine, Medical Device
W. L. Gore & Associates has announced European launch of improved GORE DrySeal Sheath with hydrophilic coating which allows for easier insertion and removal from blood vessels while performing endovascular repair procedures. The CE-marked ...
Tags: W.L.Gore&Associates, GORE DrySeal Sheath, hydrophilic coating
The European Union has granted CE mark to W L Gore & Associates' GORE EXCLUDER AAA Endoprosthesis new lower profile 31 mm diameter trunk-ipsilateral leg and 32 mm aortic extender components. Inserted through a catheter-based delivery ...
Tags: European Union, CE mark, Gore, Endoprosthesis Components
Cosmotec, a distribution partner of Endologix in Japan, has obtained Shonin approval from Japanese Ministry of Health, Labor and Welfare (MHLW) for its IntuiTrak Delivery system. Featuring a simplified deployment mechanism and hydrophilic ...
Tags: Cosmotec, Endologix, Japan, Shonin approval, MHLW
Aptus Endosystems, a developer of endovascular aneurysm repair (EVAR) technology, has completed $25m series BB equity financing. Aptus will use the finance to expand commercialization of its HeliFX Aortic Securement system in the US and ...
Tags: Aptus Endosystems, endovascular aneurysm repair technology
Medtronic has introduced the Endurant II AAA Stent Graft system in the US, following the US Food and Drug Administration's (FDA) approval. The Endurant II AAA Stent Graft system is designed for the treatment of abdominal aortic aneurysms ...
Tags: Medtronic, Endurant II AAA Stent Graft system, FDA, EVAR
Endologix, a developer of cardiovascular devices, has obtained CE mark approval for its Nellix endovascular aneurysm sealing system. The system is designed to simplify endovascular procedures and to treat patients with abdominal aortic ...
Tags: Endologix, Nellix endovascular aneurysm sealing system
The European Union has granted CE mark to W.L.Gore&Associates'endovascular stent-graft with a new 35 mm trunk-ipsilateral leg and 36 mm aortic extender. Inserted through a catheter-based delivery technique,the GORE EXCLUDER AAA ...
Tags: GORE, European Union, CE mark, aortic business