The following data is part of a premarket notification filed by Jeil Medical Corporation with the FDA for Arix Foot System.
Device ID | K161864 |
510k Number | K161864 |
Device Name: | ARIX Foot System |
Classification | Plate, Fixation, Bone |
Applicant | JEIL MEDICAL CORPORATION #702 KOLON SCIENCE VALLEY 2ND, 55, DIGITAL-RO 34, GURO-GU Seoul, KR 152-728 |
Contact | Sejin Ryu |
Correspondent | Sejin Ryu JEIL MEDICAL CORPORATION #702 KOLON SCIENCE VALLEY 2ND, 55, DIGITAL-RO 34, GURO-GU Seoul, KR 152-728 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-07-07 |
Decision Date | 2016-08-02 |
Summary: | summary |