MODIFICATION TO CONTOUR POLARIS URETERAL STENT

MODIFICATION TO CONTOUR POLARIS URETERAL STENT is an FDA 510(k)-cleared medical device (K030503) 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 March 16, 2003. Regulation: 8.