Clearance Summary
Avanti Distal Elbow ORIF System received FDA 510(k) clearance under submission number K261145, sponsored by Avanti Orthopaedics, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2026-05-09.
- Submission: K261145
- Applicant / Sponsor: Avanti Orthopaedics, LLC
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2026-05-09
Classification & Regulation
This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.