Clearance Summary
Fix2Lock(Biocomposite medial, lateral, Biocombi Self Punching) received FDA 510(k) clearance under submission number K231326, sponsored by Osteonic Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-05-31.
- Submission: K231326
- Applicant / Sponsor: Osteonic Co., Ltd.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2023-05-31
Classification & Regulation
This clearance is catalogued under FDA product code MAI and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.