WHITESIDE ORTHOLOC (TM)

WHITESIDE ORTHOLOC (TM) is an FDA 510(k)-cleared medical device (K864070) manufactured by Dow Corning Wright. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 26, 1987. Regulation: 8.