SURESHOT Distal Targeting System V4.0 Trauma Interface

SURESHOT Distal Targeting System V4.0 Trauma Interface is an FDA 510(k)-cleared medical device (K170977) manufactured by Smith & Nephew, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 2, 2017. Regulation: 8.