DYONICS INTELIJET INFLOW/OUTFLOW CANNULA

DYONICS INTELIJET INFLOW/OUTFLOW CANNULA is an FDA 510(k)-cleared medical device (K981156) manufactured by Smith & Nephew, 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 May 19, 1998. Regulation: 8.