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YAMAHACHI PMMA DISKS

K151764 Class II Traditional
Decision Date
2015-11-23
Sponsor / Applicant
Yamahachi Dental Products USA, Inc.

Technical Specification

510(k) Submission ID K151764
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2015-11-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

YAMAHACHI PMMA DISKS received FDA 510(k) clearance under submission number K151764, sponsored by Yamahachi Dental Products USA, 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 2015-11-23.

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.