meddevicedb.com FDA Device Reference

NEODONTICS DENTAL IMPLANT

K821025 Class II Traditional
Decision Date
1982-08-30
Sponsor / Applicant
Neodontics, Inc.

Technical Specification

510(k) Submission ID K821025
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1982-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEODONTICS DENTAL IMPLANT received FDA 510(k) clearance under submission number K821025, sponsored by Neodontics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1982-08-30.

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.