meddevicedb.com FDA Device Reference

KATANA Zirconia Block

K170986 Class II Traditional
Decision Date
2017-07-13
Sponsor / Applicant
Kuraray Noritake Dental, Inc.

Technical Specification

510(k) Submission ID K170986
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2017-07-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KATANA Zirconia Block received FDA 510(k) clearance under submission number K170986, sponsored by Kuraray Noritake Dental, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-07-13.

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.