The following data is part of a premarket notification filed by Sewon Medix Inc. with the FDA for Ih Implant System.
Device ID | K153521 |
510k Number | K153521 |
Device Name: | IH Implant System |
Classification | Implant, Endosseous, Root-form |
Applicant | Sewon Medix Inc. #29, Sa-sang-ro, 375beon-gil, Sa-sang-gu Busan, KR 46946 |
Contact | Bum-keun Park |
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 | 2015-12-08 |
Decision Date | 2016-10-14 |
Summary: | summary |