The following data is part of a premarket notification filed by Dentium Co., Ltd. with the FDA for Dentium Co., Ltd. Implantium.
Device ID | K041368 |
510k Number | K041368 |
Device Name: | DENTIUM CO., LTD. IMPLANTIUM |
Classification | Implant, Endosseous, Root-form |
Applicant | DENTIUM CO., LTD. 5536 TROWBRIDGE DRIVE Dunwoody, GA 30338 |
Contact | Cathryn N Cambria |
Correspondent | Cathryn N Cambria DENTIUM CO., LTD. 5536 TROWBRIDGE DRIVE Dunwoody, GA 30338 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-05-24 |
Decision Date | 2004-07-29 |
Summary: | summary |