Clearance Summary
Sentio Ti Implant Kit; Sentio 1 Mini; Genie Medical BAHS received FDA 510(k) clearance under submission number K240614, sponsored by Oticon Medical AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2024-07-10.
- Submission: K240614
- Applicant / Sponsor: Oticon Medical AB
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.3340
- Decision date: 2024-07-10
Classification & Regulation
This clearance is catalogued under FDA product code PFO and 21 CFR 874.3340, within the Ear, Nose, Throat review panel as a Class II device.