Clearance Summary
LEONI ORION System received FDA 510(k) clearance under submission number K160518, sponsored by Leoni Cia Cable System. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2016-07-14.
- Submission: K160518
- Applicant / Sponsor: Leoni Cia Cable System
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5770
- Decision date: 2016-07-14
Classification & Regulation
This clearance is catalogued under FDA product code JAI and 21 CFR 892.5770, within the Radiology review panel as a Class II device.