meddevicedb.com FDA Device Reference

Metacem

K171449 Class II Traditional
Decision Date
2018-05-15
Sponsor / Applicant
Meta Biomed Co., Ltd.

Technical Specification

510(k) Submission ID K171449
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2018-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Metacem received FDA 510(k) clearance under submission number K171449, sponsored by Meta Biomed 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 2018-05-15.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.