PARAGON POSTERIOR SPINAL SYSTEM

PARAGON POSTERIOR SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K920546) manufactured by Sofamor Danek Mfg., 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 January 20, 1993. Regulation: 8.