MODIFICATION OF INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES

MODIFICATION OF INTERGARD WOVEN COLLAGEN COATED VASCULAR PROSTHESES is an FDA 510(k)-cleared medical device (K984294) manufactured by Intervascular, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 21, 1999. Regulation: 8.