meddevicedb.com FDA Device Reference

PMMA Block

K201683 Class II Traditional
Decision Date
2020-11-03
Sponsor / Applicant
Huge Dental Material Co., Ltd.

Technical Specification

510(k) Submission ID K201683
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2020-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PMMA Block received FDA 510(k) clearance under submission number K201683, sponsored by Huge Dental Material Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2020-11-03.

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.