meddevicedb.com FDA Device Reference

TDS ABUTMENT

K081460 Class II Traditional
Decision Date
2008-11-21
Sponsor / Applicant
Pou YU Biotechnology Co., Ltd.

Technical Specification

510(k) Submission ID K081460
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2008-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TDS ABUTMENT received FDA 510(k) clearance under submission number K081460, sponsored by Pou YU Biotechnology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-11-21.

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.