The following data is part of a premarket notification filed by Osstem Implant Co.,ltd with the FDA for Gs System.
| Device ID | K063861 |
| 510k Number | K063861 |
| Device Name: | GS SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | OSSTEM IMPLANT CO.,LTD 5536 TROWBRIDGE DRIVE Dunwoody, GA 30338 |
| Contact | Cathryn N Cambria |
| Correspondent | Cathryn N Cambria OSSTEM IMPLANT CO.,LTD 5536 TROWBRIDGE DRIVE Dunwoody, GA 30338 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-12-28 |
| Decision Date | 2007-09-21 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() GS SYSTEM 79203538 5388853 Live/Registered |
Lonza Ltd. 2016-11-21 |