3D Holographic Guidance, Navigation, and Control for Endovascular Aortic Repair

Inclusion Criteria

• •1. The patient meets the instructions for use (IFU) for the 24-28 mm body Cook Zenith Flex AAA bifurcated stent graft.
• •1. Adequate iliac/femoral access compatible with the required introduction system
• •2. Non aneurysmal infrarenal aortic segment (neck) proximal to the aneurysm:
• •i. With a length of at least 15mm ii. With a diameter measured outer wall to outer wall of no greater than 26mm and no less than 20mm iii. With an angle less than 60 degrees relative to the long access of the aneurysm and iv. With an angle less than 45 degrees relative to the axis of the suprarenal aorta c. Iliac artery distal fixation site greater than 10mm in length and 7.5-20mm in diameter (measured outerwall to outerwall).
• •2. Male/female, aged ≥ 18
• •3. Patient fulfilling criteria for needing endovascular repair of abdominal aortic aneurysm according to routine clinical practice criteria of the participating center
• •4. Women of childbearing potential must be non-pregnant, non-lactating, and not planning to become pregnant during the course of the trial; and have a negative urine or serum pregnancy test within 7 days prior to index procedure
• •5. Provide written informed consent as applicable and defined by site country regulation
• •6. Stated willingness to comply with all study procedures and availability for the duration of the study