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# BioStable Science Aortic Annuplasty Device Cleared
- URL: https://www.fdaweb.com/biostable-science-aortic-annuplasty-device-cleared/
- Published: 2017-03-24T12:00:00.000Z
- Updated: 2026-09-14T22:13:44.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5138287

FDA has cleared a BioStable Science & Engineering 510(k) for the HAART 300 Aortic Annuloplasty device, designed for aortic valve repair. It is intended to re-size, reshape, and stabilize the aortic annulus to “restore valve competence and help prevent recurrent aortic regurgitation,” according to the company. “Valve repair is the gold standard surgical treatment in mitral and tricuspid valve disease because of the proven patient benefits over valve replacement.”