The purpose of this investigational trial is to establish the safety and effectiveness of a new device and delivery systems in patients with aortic stenosis (narrowing of the aortic valve resulting in obstructed blood flow).
Adults with severe, symptomatic aortic stenosis and would benefit from valve implantation may be eligible for the trial. In addition, adults with stenosed or insufficient bioprosthetic valve in any position may be eligible for the registry. Please contact the study coordinator for specific inclusion and exclusion criteria.