Clearance Summary
SURELIFT PROLAPSE SYSTEM received FDA 510(k) clearance under submission number K102815, sponsored by Neomedic International. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2011-07-07.
- Submission: K102815
- Applicant / Sponsor: Neomedic International
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class III
- Regulation citation: 21 CFR 884.5980
- Decision date: 2011-07-07
Classification & Regulation
This clearance is catalogued under FDA product code OTP and 21 CFR 884.5980, within the Obstetrics/Gynecology review panel as a Class III device.