meddevicedb.com FDA Device Reference

THE GUIDED SURGERY CONCEPT

K050393 Class II Traditional
Decision Date
2005-05-04
Sponsor / Applicant
Nobel Biocare AB

Technical Specification

510(k) Submission ID K050393
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2005-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE GUIDED SURGERY CONCEPT received FDA 510(k) clearance under submission number K050393, sponsored by Nobel Biocare AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-05-04.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.