meddevicedb.com FDA Device Reference

I-MINI DENTAL IMPLANT

K080115 Class II Traditional
Decision Date
2008-05-30
Sponsor / Applicant
Oco Biomedical

Technical Specification

510(k) Submission ID K080115
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2008-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I-MINI DENTAL IMPLANT received FDA 510(k) clearance under submission number K080115, sponsored by Oco Biomedical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-05-30.

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.