WHITESIDE BIOMECHANICS SPINAL SYSTEM

WHITESIDE BIOMECHANICS SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K991678) manufactured by Whiteside Biomechanics, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 11, 1999. Regulation: 8.