Clearance Summary
FLEXMEDICS NITINOL ARCH WIRE received FDA 510(k) clearance under submission number K863742, sponsored by Flexmedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1986-11-24.
- Submission: K863742
- Applicant / Sponsor: Flexmedics
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.5410
- Decision date: 1986-11-24
Classification & Regulation
This clearance is catalogued under FDA product code DZC and 21 CFR 872.5410, within the Dental review panel as a Class I device.