Next-generation balloon-expandable TAVR valve receives FDA approval
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Edwards Lifesciences announced its next-generation balloon-expandable valve has received approval from the FDA for transcatheter aortic valve replacement in patients with severe, symptomatic aortic stenosis at intermediate or greater risk for open-heart surgery.
As Cardiology Today’s Intervention previously reported, the next generation balloon-expandable valve (Sapien 3 Ultra) previously received clearance for use in Europe in November.
“The advanced Sapien 3 Ultra system features enhancements on the valve and a new delivery system to address the needs of both patients and clinicians, building on our best-in-class performance of Sapien 3 to further advance and improve patient care,” Larry L. Wood, Edwards’ corporate vice president, transcatheter heart valves, said in a press release. “We look forward to introducing the Sapien 3 Ultra system to U.S. patients.”
“The Edwards Sapien 3 Ultra system provides meaningful technology improvements that help further optimize the transcatheter aortic valve replacement procedure, adding simplicity and advancing patient care,” John G. Webb, MD, director of interventional cardiology and cardiac catheterization laboratories at St. Paul’s Hospital, in Vancouver, and professor of cardiology at the University of British Columbia, said in the release. – by Earl Holland Jr.
Disclosure: Webb reports he is a consultant for Edwards Lifesciences. Wood is an employee of Edwards Lifesciences.