SYNTHES POSTERIOR UNIVERSAL SPINAL SYSTEM

SYNTHES POSTERIOR UNIVERSAL SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K982987) manufactured by Synthes Spine. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 20, 1998. Regulation: 8.