Clearance Summary
CoLink® & CoLag® Non-Sterile Screws received FDA 510(k) clearance under submission number K261154, sponsored by In2Bones USA, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2026-05-30.
- Submission: K261154
- Applicant / Sponsor: In2Bones USA, LLC
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2026-05-30
Classification & Regulation
This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.