The following data is part of a premarket notification filed by Kj Meditech Co., Ltd. with the FDA for Kj External Implant System.
Device ID | K140051 |
510k Number | K140051 |
Device Name: | KJ EXTERNAL IMPLANT SYSTEM |
Classification | Implant, Endosseous, Root-form |
Applicant | KJ MEDITECH CO., LTD. 2651 E CHAPMAN AVE STE 110 Fullerton, CA 92831 |
Contact | Priscilla Chung |
Correspondent | Priscilla Chung KJ MEDITECH CO., LTD. 2651 E CHAPMAN AVE STE 110 Fullerton, CA 92831 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-01-09 |
Decision Date | 2014-10-30 |
Summary: | summary |