Clearance Summary
Benefix Interspinous Fixation System received FDA 510(k) clearance under submission number K143631, sponsored by U&I Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-09-03.
- Submission: K143631
- Applicant / Sponsor: U&I Corporation
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3050
- Decision date: 2015-09-03
Classification & Regulation
This clearance is catalogued under FDA product code PEK and 21 CFR 888.3050, within the Orthopedic review panel as a Class II device.