Journal of Vascular and Interventional Radiology
Volume 19, Issue 6, Supplement , Pages S9-S17, June 2008

Food and Drug Administration–approved Endovascular Repair Devices for Abdominal Aortic Aneurysms: A Review

Division of Cardiovascular Medicine, University of California Davis Medical Center, 4860 Y Street, Suite 2820, Sacramento, CA 95817.

Received 2 December 2007; received in revised form 10 December 2007; accepted 10 December 2007.

Endovascular treatment of infrarenal abdominal aortic aneurysm (AAA) offers a less invasive alternative to conventional open repair. Currently, only four devices are Food and Drug Administration (FDA)–approved for use in endovascular aneurysm repair (EVAR) of AAA in the United States. All four devices are associated with a high technical success rate and less morbidity than open surgical repair. Each device has its inherent design advantages and disadvantages that must be matched with patient and AAA characteristics. This review will discuss and compare the technology and procedural outcomes data of the current FDA-approved EVAR devices.

Abbreviations: AAA, abdominal aortic aneurysm, EVAR, endovascular aneurysm repair, FDA, Food and Drug Administration

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 J.R.L. serves on the advisory boards of Cordis (Warren, NJ), Boston Scientific (Natick, MA), Medtronic (Sunnyvale, CA), ev3 (Plymouth, MN), and Edwards Lifesciences (Irvine, CA).

PII: S1051-0443(08)00005-5

doi:10.1016/j.jvir.2007.12.452

Journal of Vascular and Interventional Radiology
Volume 19, Issue 6, Supplement , Pages S9-S17, June 2008