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DYRACT CEM PLUS CEMENT

K041272 Class II Traditional
Decision Date
2004-10-18
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K041272
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2004-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DYRACT CEM PLUS CEMENT received FDA 510(k) clearance under submission number K041272, sponsored by Dentsply Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2004-10-18.

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.