The following data is part of a premarket notification filed by Dentium Co., Ltd. with the FDA for Implantium Prosthetics.
Device ID | K052957 |
510k Number | K052957 |
Device Name: | IMPLANTIUM PROSTHETICS |
Classification | Abutment, Implant, Dental, Endosseous |
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 | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-10-21 |
Decision Date | 2006-07-27 |
Summary: | summary |