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NEW STETIC ACRYLICS

K102874 Class II Traditional
Decision Date
2011-03-28
Sponsor / Applicant
New Stetic

Technical Specification

510(k) Submission ID K102874
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 2011-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEW STETIC ACRYLICS received FDA 510(k) clearance under submission number K102874, sponsored by New Stetic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2011-03-28.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.