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Beasley, MD, Robert L. Feldman, MD, Charles S. Thompson, MD, and James B. Williams, MD. Conducted at eight U.S. Centers per FDA regulations and international clinical trials standards, the 44-patient trial was made to measure the safety and performance of the Powerlink stent graft with a suprarenal aortic extension.S. Meals and Drug Administration acceptance of the device and treatment algorithm in 2009 2009, and recent FDA and European CE Tag approvals of the PowerFit suprarenal aortic expansion this year. John McDermott, President and Chief Executive Officer said, ‘We are very happy to announce these excellent results from our suprarenal trial, which build on the very similar published outcomes from our initial FDA trial, and the Powerlink XL trial. As the shift from open surgery to endovascular repair evolves, we expect to continue to reap the benefits of being the only organization that offers doctors both infrarenal and suprarenal configurations together with the unique benefits of the anatomical fixation technique.’..