Clearance Summary
FiberLocker Implant ; FiberLocker Instrument ; FiberLocker PowerUnit received FDA 510(k) clearance under submission number K253867, sponsored by ZuriMED Technologies AG. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2026-01-02.
- Submission: K253867
- Applicant / Sponsor: ZuriMED Technologies AG
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3300
- Decision date: 2026-01-02
Classification & Regulation
This clearance is catalogued under FDA product code OWX and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.