The following data is part of a premarket notification filed by Neobiotech Co., Ltd. with the FDA for Is-iii Hactive Fixture.
Device ID | K173938 |
510k Number | K173938 |
Device Name: | IS-III HActive Fixture |
Classification | Implant, Endosseous, Root-form |
Applicant | Neobiotech Co., Ltd. #312-1, 36, Digital-ro 27-gil, Guro-gu Seoul, KR 08381 |
Contact | Young-ko Heo |
Correspondent | April Lee Withus Consulting Inc 106 Superior Irvine, CA 92620 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-12-26 |
Decision Date | 2018-05-24 |
Summary: | summary |