SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE

SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE is an FDA 510(k)-cleared medical device (K034012) 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 March 15, 2004. Regulation: 8.