Clearance Summary
Catamaran SI Joint Fusion System received FDA 510(k) clearance under submission number K250403, sponsored by Tenon Medical. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2025-03-21.
- Submission: K250403
- Applicant / Sponsor: Tenon Medical
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2025-03-21
Classification & Regulation
This clearance is catalogued under FDA product code OUR and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.