CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000

CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000 is an FDA 510(k)-cleared medical device (K980588) manufactured by Clarus Medical Systems, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 17, 1998. Regulation: 8.