Medtronic Garners First-Of-Its-Kind FDA Approval for 'AUI' Device with Endurant II AAA Stent Graft System
Global Market-Leader in Medical Technology for Endovascular Aortic Repair
Also Receives 510(k) Clearance for Sentrant Introducer Sheath
MINNEAPOLIS -- May 30, 2013 -- Medtronic, Inc. (MDT) is expanding its market-leading portfolio of products for endovascular aortic repair in the United States with two new medical devices: the company recently received approval from the U.S. Food and Drug Administration (FDA) for the Endurant II Aorto-Uni-Iliac (AUI) Stent Graft System and the FDA`s 510(k) clearance for the Sentrant Introducer Sheath; both devices will be on exhibit at the Medtronic booth during the Society for Vascular Surgery`s "Vascular Annual Meeting," which runs May 30-June 2 in San Francisco.
- Published: 30 May 2013
- Written by Editor