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 |