AUTO SUTURE KERRISON SPINAL RONGEUR

AUTO SUTURE KERRISON SPINAL RONGEUR is an FDA 510(k)-cleared medical device (K943116) manufactured by United States Surgical, A Division of Tyco Healthc. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 26, 1994. Regulation: 8.