The following data is part of a premarket notification filed by Osstem Implant Co., Ltd.. with the FDA for Ossbuilder System.
Device ID | K172354 |
510k Number | K172354 |
Device Name: | OssBuilder System |
Classification | Plate, Bone |
Applicant | Osstem Implant Co., Ltd.. 66-16, Bansong-ro 513beon-gil, Haeundae-gu Busan, KR 612-070 |
Contact | Jungmin Yoo |
Correspondent | David Kim Hiossen Inc. 85 Ben Fairless Dr. Fairless Hills, PA 19030 |
Product Code | JEY |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-08-03 |
Decision Date | 2018-03-26 |
Summary: | summary |