JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II)

JOHNSON & JOHNSON POSTERIOR DENTAL (ADAPTIC II) is an FDA 510(k)-cleared medical device (K841518) manufactured by Johnson & Johnson Professionals, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 20, 1984. Regulation: 8.