The following data is part of a premarket notification filed by Jeil Medical Corporation with the FDA for Arix Diaphysis System.
| Device ID | K171285 |
| 510k Number | K171285 |
| Device Name: | ARIX Diaphysis 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 | Yein Han |
| Correspondent | Yein Han 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 | 2017-05-01 |
| Decision Date | 2017-07-24 |
| Summary: | summary |