meddevicedb.com FDA Device Reference

NEODENT IMPLANT SYSTEM

K133696 Class II Traditional
Decision Date
2014-02-25
Sponsor / Applicant
Jjgc Industria E Comercio DE Materiais Dentarios S

Technical Specification

510(k) Submission ID K133696
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2014-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEODENT IMPLANT SYSTEM received FDA 510(k) clearance under submission number K133696, sponsored by Jjgc Industria E Comercio DE Materiais Dentarios S. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2014-02-25.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.