Clearance Summary
EndoRotor received FDA 510(k) clearance under submission number K170120, sponsored by Interscope, Inc.. 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 2017-04-18.
- Submission: K170120
- Applicant / Sponsor: Interscope, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1690
- Decision date: 2017-04-18
Classification & Regulation
This clearance is catalogued under FDA product code PTE and 21 CFR 884.1690, within the Obstetrics/Gynecology review panel as a Class II device.