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 |