DANEK(TM) SPINAL EPIDURAL ENDOSCOPIC SY

DANEK(TM) SPINAL EPIDURAL ENDOSCOPIC SY is an FDA 510(k)-cleared medical device (K930191) manufactured by Sofamor Danek Mfg., Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 25, 1995. Regulation: 8.