Clearance Summary
Origin Anterior Cervical Plate System received FDA 510(k) clearance under submission number K193494, sponsored by Orthopaedic & Spine Development. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2020-04-06.
- Submission: K193494
- Applicant / Sponsor: Orthopaedic & Spine Development
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3060
- Decision date: 2020-04-06
Classification & Regulation
This clearance is catalogued under FDA product code KWQ and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.