SEURAT™ Universal Pedicle Screw System

SEURAT™ Universal Pedicle Screw System is an FDA 510(k)-cleared medical device (K173185) manufactured by Ctl Medical Corporation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 13, 2018. Regulation: 8.