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 |