meddevicedb.com FDA Device Reference

Multi-unit Abutment Plus

K161416 Class II Traditional
Decision Date
2017-03-16
Sponsor / Applicant
Nobel Biocare AB

Technical Specification

510(k) Submission ID K161416
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2017-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Multi-unit Abutment Plus received FDA 510(k) clearance under submission number K161416, sponsored by Nobel Biocare AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-03-16.

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.