Clearance Summary
ROVERS SPATULA received FDA 510(k) clearance under submission number K002520, sponsored by Rovers Medical Devices B.V.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2000-11-13.
- Submission: K002520
- Applicant / Sponsor: Rovers Medical Devices B.V.
- Clearance pathway: Abbreviated
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4530
- Decision date: 2000-11-13
Classification & Regulation
This clearance is catalogued under FDA product code HHT and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.