The following data is part of a premarket notification filed by Dentis Co. Ltd. with the FDA for Modificaton To: Dentis Dental Implant System.
Device ID | K082843 |
510k Number | K082843 |
Device Name: | MODIFICATON TO: DENTIS DENTAL IMPLANT SYSTEM |
Classification | Implant, Endosseous, Root-form |
Applicant | DENTIS CO. LTD. 13340 E FIRESTONE BLVD SUITE J Santa Fe Springs, CA 90670 |
Contact | Jung Bae Bang |
Correspondent | Jung Bae Bang DENTIS CO. LTD. 13340 E FIRESTONE BLVD SUITE J Santa Fe Springs, CA 90670 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-09-29 |
Decision Date | 2009-06-19 |
Summary: | summary |