RENOVIS T 710 LARGE EXTERNAL FIXATION SYSTEM

RENOVIS T 710 LARGE EXTERNAL FIXATION SYSTEM is an FDA 510(k)-cleared medical device (K110965) manufactured by Renovis Surgical Technologies, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 10, 2011. Regulation: 8.