Clearance Summary
ORTHODONTIC ARCH received FDA 510(k) clearance under submission number K872622, sponsored by Wonder Wire. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1987-10-09.
- Submission: K872622
- Applicant / Sponsor: Wonder Wire
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4565
- Decision date: 1987-10-09
Classification & Regulation
This clearance is catalogued under FDA product code EJZ and 21 CFR 872.4565, within the Dental review panel as a Class I device.