SYNTHES (U.S.A.) UNIVERSAL SPINAL PARALLEL CONNECTOR

SYNTHES (U.S.A.) UNIVERSAL SPINAL PARALLEL CONNECTOR is an FDA 510(k)-cleared medical device (K962608) manufactured by Synthes (Usa). This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 8, 1996. Regulation: 8.