The following data is part of a premarket notification filed by Dentium Co., Ltd. with the FDA for Dentium Implantium & Superline Prosthetics.
Device ID | K160828 |
510k Number | K160828 |
Device Name: | Dentium Implantium & SuperLine Prosthetics |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | DENTIUM CO., LTD. 150, EONDONG-RO, GIHEUNG-GU Yongin-si, KR 443-270 |
Contact | Sangpil Yoon |
Correspondent | Sangpil Yoon DENTIUM CO., LTD. 150, EONDONG-RO, GIHEUNG-GU Yongin-si, KR 443-270 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-03-25 |
Decision Date | 2016-09-15 |
Summary: | summary |