KIVA VCF TREATMENT SYSTEM

KIVA VCF TREATMENT SYSTEM is an FDA 510(k)-cleared medical device (K132817) manufactured by Benvenue Medical, 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 23, 2014. Regulation: 8.