KARL STORZ SLOTTED WHISKER ARTHROSCOPIC BLADE

KARL STORZ SLOTTED WHISKER ARTHROSCOPIC BLADE is an FDA 510(k)-cleared medical device (K963029) manufactured by KARL STORZ Endoscopy-America, 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 November 26, 1996. Regulation: 8.