meddevicedb.com FDA Device Reference

4plus6Line Abutment System

K151608 Class II Traditional
Decision Date
2016-04-13
Sponsor / Applicant
Ot Medical GmbH

Technical Specification

510(k) Submission ID K151608
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2016-04-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

4plus6Line Abutment System received FDA 510(k) clearance under submission number K151608, sponsored by Ot Medical GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-04-13.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.