BioStable Science & Engineering Announces the First Commercial Use of the HAART 200™ Aortic Annuloplasty Device

BioStable Science & Engineering, Inc. announced today the first commercial use of the HAART 200 Aortic Annuloplasty Device in the U.S. by doctors at the West Virginia University (WVU) Heart and Vascular Institute in Morgantown, West Virginia. Drs. Lawrence Wei, Vinay Badhwar and J. Scott Rankin were the collaborating surgeons for the procedure. The HAART 200 Aortic Annuloplasty Device is the only FDA cleared annuloplasty device designed to facilitate bicuspid aortic valve repair. The WVU Heart and Vascular Institute is the first of a select group of centers expected to participate in a limited release of the product this year. (Read More)