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HYBRID ENDOPORE ENDOSSEOUS DENTAL IMPLANT

K040714 Class II Special
Decision Date
2004-04-09
Sponsor / Applicant
Innova Corp.

Technical Specification

510(k) Submission ID K040714
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2004-04-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYBRID ENDOPORE ENDOSSEOUS DENTAL IMPLANT received FDA 510(k) clearance under submission number K040714, sponsored by Innova Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2004-04-09.

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.