Pinnacle Lite Pelvic Floor Repair Kit, Posterior Uphold Lite Vaginal Support System

K122459 is the FDA 510(k) clearance record for PINNACLE LITE PELVIC FLOOR REPAIR KIT, POSTERIOR UPHOLD LITE VAGINAL SUPPORT SYSTEM, a class III device, cleared for Boston Scientific Corporation on 2012-12-13 under FDA product code OTP (Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed). FDA's definition for product code OTP reads: "Tissue reinforcement of the fibromuscular layer of the pelvic floor when surgical treatment is indicated; Procedures include anterior and posterior vaginal wall prolapse repair and vaginal apical or uterine prolapse repair performed...". FDA records list 1,110 510(k) clearances for Boston Scientific Corporation, from 1988-11-23 to 2026-08-12. As of 2026-09-10, FDA records show 2 recalls naming K122459.