The following data is part of a premarket notification filed by Osstem Implant Co., Ltd. with the FDA for Et Us Ss Prosthetic System.
Device ID | K160670 |
510k Number | K160670 |
Device Name: | ET US SS Prosthetic System |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | OSSTEM IMPLANT CO., LTD. #507-8 GEOJE3-DONG YEONJE-GU Busan, KR 611-804 |
Contact | Hee Kwon |
Correspondent | David Kim HIOSSEN INC. 85 BEN FAIRLESS DR. Fairless Hills, PA 19030 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-03-10 |
Decision Date | 2017-04-25 |
Summary: | summary |