WRIGHT PLASTER OF PARIS BONE VOID FILLER KIT (SUBJECT TO REVISION)

WRIGHT PLASTER OF PARIS BONE VOID FILLER KIT (SUBJECT TO REVISION) is an FDA 510(k)-cleared medical device (K963587) 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 March 23, 1997. Regulation: 8.