The following data is part of a premarket notification filed by Osstem Implant Co., Ltd. with the FDA for Osstem Abutment System.
Device ID | K182091 |
510k Number | K182091 |
Device Name: | Osstem Abutment System |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | Osstem Implant Co., Ltd. 66-16, Bansong-ro 513beon-gil, Haeundae-gu Busan, KR 612-070 |
Contact | Jungmin Yoo |
Correspondent | Peter Lee 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 | 2018-08-03 |
Decision Date | 2019-07-12 |