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Surgeons Complete Clinical Trial on Novel Two-Part Heart Valve
Date:6/11/2013

ct's compliance with European Union requirements, and enables the free movement of products within the European Economic Area. ValveXchange will also implement the process for FDA clearance in the United States.

“This milestone represents a major achievement for ValveXchange,” says Parrish. “The completion of enrollment in the VITAL-2 trial, and the best-in-class valve performance results, substantiate the ValveXchange philosophy that better science equals better valves.”

Vitality Heart Valve System
The ValveXchange system includes a two-part valve with a permanently implanted base and an easily replaceable leaflet set. Surgeons can replace the leaflet set transapically (through the apex of the heart), accessing it by a small incision between the ribs. The system’s design allows surgeons to replace leaflets with standard, minimally invasive surgical techniques that are faster and simpler than traditional redo valve replacement surgeries, while restoring top performance at the same time.

ValveXchange heart valves provide excellent hemodynamics, long durability and leaflet exchangeability, and are easy to implant, according to Ivan Vesely, Ph.D., heart valve scientist and founder of ValveXchange. “The Vitality Heart Valve System offers simplicity, security and unprecedented visibility into the aortic space,” he says. “The hemodynamics of the Vitality valves – are excellent, particularly in the smaller valve sizes.”

ValveXchange®, Inc. (http://www.valvexchange.com)
ValveXchange®, Inc. is an emerging medical technology company serving cardiac surgeons and cardiologists. The company is the developer of the Vitality Heart Valve System™, the first serviceable bioprosthetic heart valve. The company’s family of products also includes the Vitality-S™ sutureless valve, ideal for minimally invasive and robotic implants, and
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