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Magic UCLA Abutment System

K202418 Class II Special
Decision Date
2020-12-03
Sponsor / Applicant
Innobiosurg Co., Ltd.

Technical Specification

510(k) Submission ID K202418
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2020-12-03
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Magic UCLA Abutment System received FDA 510(k) clearance under submission number K202418, sponsored by Innobiosurg Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2020-12-03.

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.