meddevicedb.com FDA Device Reference

TruAbutment DS, TruBase

K203649 Class II Traditional
Decision Date
2021-09-15
Sponsor / Applicant
Truabutment, Inc.

Technical Specification

510(k) Submission ID K203649
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2021-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TruAbutment DS, TruBase received FDA 510(k) clearance under submission number K203649, sponsored by Truabutment, 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 2021-09-15.

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.