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 |