PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEM

PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K132884) manufactured by Zimmer Spine, 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 November 24, 2013. Regulation: 8.