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OSSEOTITE DENTAL IMPLANTS

K983347 Class II Traditional
Decision Date
1999-01-06
Sponsor / Applicant
Implant Innovations, Inc.

Technical Specification

510(k) Submission ID K983347
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1999-01-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSSEOTITE DENTAL IMPLANTS received FDA 510(k) clearance under submission number K983347, sponsored by Implant Innovations, 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 1999-01-06.

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.