meddevicedb.com FDA Device Reference

INCORIS ZI

K062509 Class II Traditional
Decision Date
2006-09-12
Sponsor / Applicant
Sirona Dental Systems GmbH

Technical Specification

510(k) Submission ID K062509
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2006-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INCORIS ZI received FDA 510(k) clearance under submission number K062509, sponsored by Sirona Dental Systems GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-09-12.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.