meddevicedb.com FDA Device Reference

TI-MAX X450

K112024 Class I Traditional
Decision Date
2012-06-20
Sponsor / Applicant
Nakanishi, Inc.

Technical Specification

510(k) Submission ID K112024
Product Code EFB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2012-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TI-MAX X450 received FDA 510(k) clearance under submission number K112024, sponsored by Nakanishi, 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 2012-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code EFB and 21 CFR 872.4200, within the Dental review panel as a Class I device.