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 |