meddevicedb.com FDA Device Reference

TRUBYTE DENTURE BASE RESIN SYSTEM

K011560 Class II Traditional
Decision Date
2001-07-12
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K011560
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 2001-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRUBYTE DENTURE BASE RESIN SYSTEM received FDA 510(k) clearance under submission number K011560, 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 2001-07-12.

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.