SUNDT-KEES REINFORCING ANEURYSM CLIP

SUNDT-KEES REINFORCING ANEURYSM CLIP is an FDA 510(k)-cleared medical device (K844352) manufactured by Kees Surgical Specialty Co., Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 23, 1985. Regulation: 8.