SYNERGY TI ANTERIOR SPINAL SYSTEM

SYNERGY TI ANTERIOR SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K950709) manufactured by Cross Medical Products, 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 October 24, 1995. Regulation: 8.