WALLSTENT ENTERAL ENDOPROSTHESIS

WALLSTENT ENTERAL ENDOPROSTHESIS is an FDA 510(k)-cleared medical device (K980113) manufactured by Boston Scientific Scimed, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 2, 1998. Regulation: 8.