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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Implant, Endosseous, Root-Form
510(k) Number K173938
Device Name IS-III HActive Fixture
Applicant
Neobiotech Co., Ltd.
#312-1, 36, Digital-Ro 27-Gil, Guro-Gu
Seoul,  KR 08381
Applicant Contact Young-Ko Heo
Correspondent
Withus Consulting, Inc.
106 Superior
Irvine,  CA  92620
Correspondent Contact April Lee
Regulation Number872.3640
Classification Product Code
DZE  
Subsequent Product Code
NHA  
Date Received12/26/2017
Decision Date 05/24/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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