meddevicedb.com FDA Device Reference

CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS

K960021 Class II Traditional
Decision Date
1996-02-08
Sponsor / Applicant
Calcitek, Inc.

Technical Specification

510(k) Submission ID K960021
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1996-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS received FDA 510(k) clearance under submission number K960021, sponsored by Calcitek, 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 1996-02-08.

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.