meddevicedb.com FDA Device Reference

ULTRACROWN 75 ALLOY

K032851 Class II Special
Decision Date
2003-09-26
Sponsor / Applicant
Dentsply International

Technical Specification

510(k) Submission ID K032851
Product Code EJT
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3060
Decision Date 2003-09-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRACROWN 75 ALLOY received FDA 510(k) clearance under submission number K032851, sponsored by Dentsply International. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code EJT and 21 CFR 872.3060, within the Dental review panel as a Class II device.