Clearance Summary
TECHFIT Patient-Specific Cranial System received FDA 510(k) clearance under submission number K250297, sponsored by Techfit Digital Surgery, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2025-10-27.
- Submission: K250297
- Applicant / Sponsor: Techfit Digital Surgery, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5320
- Decision date: 2025-10-27
Classification & Regulation
This clearance is catalogued under FDA product code GWO and 21 CFR 882.5320, within the Neurology review panel as a Class II device.