GENERATION 5 LINKOW BLADE IMPLANTS

GENERATION 5 LINKOW BLADE IMPLANTS is an FDA 510(k)-cleared medical device (K822969) manufactured by Leonard P. Linkow, D.D.L.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 3, 1982. Regulation: 8.