GYNECARE PROLIFT +M* PELVIC FLOOR REPAIR SYSTEMS

GYNECARE PROLIFT +M* PELVIC FLOOR REPAIR SYSTEMS is an FDA 510(k)-cleared medical device (K071512) manufactured by ETHICON, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on May 14, 2008. Regulation: 8.