Observational study to determine safety and efficacy of the HeliFX Aortic Securement System.
Patients undergoing endovascular repair of abdominal aortic aneurysms, or patients undergoing repair of an endoleak or migration after endovascular repair of abdominal aortic aneurysm.
This is an observational study of an FDA-approved device. Data is collected from regular standard care implant and follow-up.
Patients are followed for five years.
Tiffany Whitaker, RN (217) 545-2531 or email@example.com
Kim Hodgson, MD