PATHWAY STM-10 PELVIC FLOOR STIMULATOR

PATHWAY STM-10 PELVIC FLOOR STIMULATOR is an FDA 510(k)-cleared medical device (K030039) manufactured by The Prometheus Group. 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 22, 2003. Regulation: 8.