BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM

BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM is an FDA 510(k)-cleared medical device (K130298) manufactured by Biopro, 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 June 17, 2013. Regulation: 8.