WALLSTENT BILIARY ENDOPROSTHESIS

WALLSTENT BILIARY ENDOPROSTHESIS is an FDA 510(k)-cleared medical device (K000308) manufactured by Boston Scientific Corp. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 18, 2000. Regulation: 8.