Smith & Nephew SURESHOT Distal Targeting System V4.0

Smith & Nephew SURESHOT Distal Targeting System V4.0 is an FDA 510(k)-cleared medical device (K170280) 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 27, 2017. Regulation: 8.