Smith & Nephew SURESHOT Distal Targeting System V4.0 Targeter

Smith & Nephew SURESHOT Distal Targeting System V4.0 Targeter is an FDA 510(k)-cleared medical device (K180277) 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 April 23, 2018. Regulation: 8.