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NEODENT IMPLANT SYSTEM

K133510 Class II Traditional
Decision Date
2014-02-24
Sponsor / Applicant
Jj Industria E Comercio DE Materiais Dentarios SA

Technical Specification

510(k) Submission ID K133510
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2014-02-24
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 K133510, sponsored by Jj Industria E Comercio DE Materiais Dentarios SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2014-02-24.

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.