Clearance Summary
LEFORTE SYSTEM BONE PLATE received FDA 510(k) clearance under submission number K091679, sponsored by Jeil Medical Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-10-02.
- Submission: K091679
- Applicant / Sponsor: Jeil Medical Corporation
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.4760
- Decision date: 2009-10-02
Classification & Regulation
This clearance is catalogued under FDA product code JEY and 21 CFR 872.4760, within the Dental review panel as a Class II device.