meddevicedb.com FDA Device Reference

PMMA CAD/CAM DISC

K112967 Class II Traditional
Decision Date
2012-08-28
Sponsor / Applicant
Polident D.O.O., Dental Products Industry

Technical Specification

510(k) Submission ID K112967
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2012-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PMMA CAD/CAM DISC received FDA 510(k) clearance under submission number K112967, sponsored by Polident D.O.O., Dental Products Industry. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code EBG and 21 CFR 872.3770, within the Dental review panel as a Class II device.