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UCLA/UNIVERSAL ABUTMENT

K993129 Class II Traditional
Decision Date
2000-03-28
Sponsor / Applicant
Diamodent

Technical Specification

510(k) Submission ID K993129
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2000-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UCLA/UNIVERSAL ABUTMENT received FDA 510(k) clearance under submission number K993129, sponsored by Diamodent. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-03-28.

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.