meddevicedb.com FDA Device Reference

Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments

K230873 Class II Traditional
Decision Date
2023-08-01
Sponsor / Applicant
Southern Implants (Pty), Ltd.

Technical Specification

510(k) Submission ID K230873
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2023-08-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments received FDA 510(k) clearance under submission number K230873, sponsored by Southern Implants (Pty), 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 2023-08-01.

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.