CENTAUR SPINAL SYSTEM

CENTAUR SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K994347) manufactured by Howmedica Osteonics Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 14, 2000. Regulation: 8.