Clearance Summary
CORIOGRAPH Pre-Op Planning and Modeling Services received FDA 510(k) clearance under submission number K250921, sponsored by Blue Belt Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2025-06-25.
- Submission: K250921
- Applicant / Sponsor: Blue Belt Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2025-06-25
Classification & Regulation
This clearance is catalogued under FDA product code PBF and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.