C-LEG (3C100)

C-LEG (3C100) is an FDA 510(k)-cleared medical device (K991590) manufactured by Otto Bock Orthopedic Industry, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 7, 1999. Regulation: 8.