The following data is part of a premarket notification filed by Megagen Implant Co., Ltd. with the FDA for Anyridge Octa 1 Implant System.
Device ID | K182448 |
510k Number | K182448 |
Device Name: | AnyRidge Octa 1 Implant System |
Classification | Implant, Endosseous, Root-form |
Applicant | MegaGen Implant Co., Ltd. 45, Secheon-ro, 7-gil, Dasa-eup, Dalesong-gun Daegu, KR |
Contact | Hyejin Jung |
Correspondent | Priscilla Chung LK Consulting Group USA, Inc. 690 Roosevelt Irvine, CA 92620 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-07 |
Decision Date | 2019-10-09 |
Summary: | summary |