K103426 is an FDA 510(k) clearance for the LITE PELVIC FLOOR REPAIR KITS, a Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed (Class III — Premarket Approval, product code OTP), submitted by Boston Scientific Corp (Marborough, US). The FDA issued a Cleared decision on September 14, 2011, 296 days after receiving the submission on November 22, 2010. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.5980.
| 510(k) Number | K103426 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 22, 2010 |
| Decision Date | September 14, 2011 |
| Days to Decision | 296 days |
| Submission Type | Abbreviated |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | OTP — Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally Placed |
| Device Class | Class III — Premarket Approval |
| CFR Regulation | 21 CFR 884.5980 |
| Definition | 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 Transvaginally |