The system uses helical anchor technology to enable independent endograft fixation. It’s designed to mimic the hand suturing performed during open surgical repair of abdominal aortic aneurysms. The system also can be used during initial EVAR procedures to enhance fixation and sealing mechanisms.
Related Articles on Device Approvals:
FDA Approves Carestream’s Vue Motion Medical Image Viewer
FDA Approval for Edwards’ Sapien Device is a First for U.S. Market
Cook Medical’s GI Stent Approved by the FDA
At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.
