RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM

RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM is an FDA 510(k)-cleared medical device (K142095) manufactured by Renovis Surgical Technologies, 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 14, 2014. Regulation: 8.