STRYKER STILETTO ELECTROSURGICAL PROBE

STRYKER STILETTO ELECTROSURGICAL PROBE is an FDA 510(k)-cleared medical device (K052141) manufactured by Stryker Endoscopy. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 5, 2005. Regulation: 8.