Clearance Summary
restor3d TiDAL Lumbar Interbody Fusion Device received FDA 510(k) clearance under submission number K220523, sponsored by Restor3D. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2022-06-17.
- Submission: K220523
- Applicant / Sponsor: Restor3D
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3080
- Decision date: 2022-06-17
Classification & Regulation
This clearance is catalogued under FDA product code MAX and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.