The following data is part of a premarket notification filed by Megagen Implant Co., Ltd. with the FDA for Anyone Onestage Implant System.
Device ID | K210161 |
510k Number | K210161 |
Device Name: | AnyOne Onestage Implant System |
Classification | Implant, Endosseous, Root-form |
Applicant | MegaGen Implant Co., Ltd. 45, Secheon-ro, 7-gil Daegu, KR 42921 |
Contact | You Jung Kim |
Correspondent | You Jung Kim DaeGyeong Regulatory Affairs Institute 32, Innovalley-ro Daegu, KR 41065 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-01-21 |
Decision Date | 2021-06-22 |
Summary: | summary |