The following data is part of a premarket notification filed by Osstem Implant Co., Ltd. with the FDA for Osstem Implant System - Abutment.
Device ID | K161689 |
510k Number | K161689 |
Device Name: | OSSTEM Implant System - Abutment |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | OSSTEM IMPLANT Co., Ltd. 66-16, Bansong-ro 513beon-gil, Haeundae-gu Busan, KR 612-070 |
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 | 2016-06-20 |
Decision Date | 2017-05-22 |
Summary: | summary |