meddevicedb.com FDA Device Reference

INION BIORESTORE

K070784 Class II Traditional
Decision Date
2007-07-24
Sponsor / Applicant
Inion OY

Technical Specification

510(k) Submission ID K070784
Product Code LYC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3930
Decision Date 2007-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INION BIORESTORE received FDA 510(k) clearance under submission number K070784, sponsored by Inion OY. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2007-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code LYC and 21 CFR 872.3930, within the Dental review panel as a Class II device.