WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION)

WRIGHT PLASTER OF PARIS PELLETS (SUBJECT TO REVISION) is an FDA 510(k)-cleared medical device (K960978) manufactured by Wrightmedicaltechnologyinc. 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 20, 1996. Regulation: 8.