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IH Implant System

K153521 Class II Traditional
Decision Date
2016-10-14
Sponsor / Applicant
Sewonmedix, Inc.

Technical Specification

510(k) Submission ID K153521
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2016-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IH Implant System received FDA 510(k) clearance under submission number K153521, sponsored by Sewonmedix, 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 2016-10-14.

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.