meddevicedb.com FDA Device Reference

SPI VARIOMULTI ANGLED ABUTMENT

K090153 Class II Traditional
Decision Date
2009-03-27
Sponsor / Applicant
Thommen Medical AG

Technical Specification

510(k) Submission ID K090153
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2009-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPI VARIOMULTI ANGLED ABUTMENT received FDA 510(k) clearance under submission number K090153, sponsored by Thommen Medical AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-03-27.

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.