meddevicedb.com FDA Device Reference

A-1103 ABUTMENT (REMOVABLE)

K903040 Class II Traditional
Decision Date
1990-11-26
Sponsor / Applicant
Minimatic Implant Technology

Technical Specification

510(k) Submission ID K903040
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1990-11-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

A-1103 ABUTMENT (REMOVABLE) received FDA 510(k) clearance under submission number K903040, sponsored by Minimatic Implant Technology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1990-11-26.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.