KARL STORZ KNIVES, CURETTS, HOOKS, PROBES

KARL STORZ KNIVES, CURETTS, HOOKS, PROBES is an FDA 510(k)-cleared medical device (K945891) 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 June 8, 1995. Regulation: 8.