The following data is part of a premarket notification filed by Megagen Implant Co., Ltd with the FDA for Mini Internal Implant System.
Device ID | K150537 |
510k Number | K150537 |
Device Name: | MiNi Internal Implant System |
Classification | Implant, Endosseous, Root-form |
Applicant | MEGAGEN IMPLANT CO., LTD 472, HANJANGGUN-RO, JAIN-MYEON Gyeongsan-si, KR 712-852 |
Contact | Dong Guk Ha |
Correspondent | Megan Hold KODENT, INC. 325 N. PUENTE ST., UNIT B Brea, CA 92821 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-03-03 |
Decision Date | 2015-07-21 |
Summary: | summary |