Clearance Summary
Spine Navigation and Robotic-Assistance Device received FDA 510(k) clearance under submission number K233228, sponsored by Ecential Robotics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2024-06-14.
- Submission: K233228
- Applicant / Sponsor: Ecential Robotics
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 2024-06-14
Classification & Regulation
This clearance is catalogued under FDA product code OLO and 21 CFR 882.4560, within the Neurology review panel as a Class II device.