The following data is part of a premarket notification filed by Osstem Implant Co.,ltd. with the FDA for Us Sa Implant System.
Device ID | K161103 |
510k Number | K161103 |
Device Name: | US SA Implant System |
Classification | Implant, Endosseous, Root-form |
Applicant | OSSTEM IMPLANT CO.,LTD. 66-16, BANSONG-RO 513BEON-GIL, HAEUDAE-GU Busan, KR 612-070 |
Contact | Hee Kwon |
Correspondent | David Kim HIOSSEN INC. 85 BEN FAIRLESS DR. Fairless Hills, PA 19030 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-04-19 |
Decision Date | 2017-02-02 |
Summary: | summary |