meddevicedb.com FDA Device Reference

SYSTEM PLUS

K073475 Class II Traditional
Decision Date
2008-03-10
Sponsor / Applicant
Continental Dental Laboratory

Technical Specification

510(k) Submission ID K073475
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2008-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYSTEM PLUS received FDA 510(k) clearance under submission number K073475, sponsored by Continental Dental Laboratory. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-03-10.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.