STRYKER VENOM ELECTRODES AND CANNULAE

STRYKER VENOM ELECTRODES AND CANNULAE is an FDA 510(k)-cleared medical device (K123178) manufactured by Stryker Instruments, Instruments Div.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 27, 2013. Regulation: 8.