meddevicedb.com FDA Device Reference

Perfit FS Dental Zirconia Fully Sintered Block

K203590 Class II Traditional
Decision Date
2021-06-24
Sponsor / Applicant
Vatech Acucera, Inc.

Technical Specification

510(k) Submission ID K203590
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2021-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Perfit FS Dental Zirconia Fully Sintered Block received FDA 510(k) clearance under submission number K203590, sponsored by Vatech Acucera, 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 2021-06-24.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.