The following data is part of a premarket notification filed by Innobiosurg Co., Ltd with the FDA for Magicore System.
Device ID | K152520 |
510k Number | K152520 |
Device Name: | Magicore System |
Classification | Implant, Endosseous, Root-form |
Applicant | INNOBIOSURG CO., LTD 44-19, Techno 10-ro, Yuseong-gu Daejeon, KR 305-510 |
Contact | Bo-reum Yoo |
Correspondent | April Lee Withus Group Inc 2531 Pepperdale Drive Rowland Heights, CA 91748 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-09-03 |
Decision Date | 2016-01-25 |
Summary: | summary |