Clearance Summary
Auxilock GFS Mini, GFS II Large, and GFS Ultimate received FDA 510(k) clearance under submission number K213018, sponsored by Auxein Medical Private Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2022-11-18.
- Submission: K213018
- Applicant / Sponsor: Auxein Medical Private Limited
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2022-11-18
Classification & Regulation
This clearance is catalogued under FDA product code MBI and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.