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EDOSSEOUS DENTAL IMPLANT

K970127 Class II Traditional
Decision Date
1997-06-23
Sponsor / Applicant
Sulzer Calcitek, Inc.

Technical Specification

510(k) Submission ID K970127
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1997-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EDOSSEOUS DENTAL IMPLANT received FDA 510(k) clearance under submission number K970127, sponsored by Sulzer 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 1997-06-23.

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.