meddevicedb.com FDA Device Reference

HERO II DENTAL IMPLANT SYSTEM, UI DENTAL IMPLANT SYSTEM

K130221 Class II Special
Decision Date
2013-03-21
Sponsor / Applicant
Medimecca Co., Ltd.

Technical Specification

510(k) Submission ID K130221
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2013-03-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HERO II DENTAL IMPLANT SYSTEM, UI DENTAL IMPLANT SYSTEM received FDA 510(k) clearance under submission number K130221, sponsored by Medimecca Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-03-21.

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.