The following data is part of a premarket notification filed by Huvexel Co., Ltd with the FDA for Fortis And Hana Anterior Cervical Plate System.
| Device ID | K173099 |
| 510k Number | K173099 |
| Device Name: | Fortis And Hana Anterior Cervical Plate System |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | Huvexel Co., Ltd 101-105 Megacenter, SK Technopark, 124, Sagimakgol-ro Jungwon-gu Seongnam-si, KR 13207 |
| Contact | Sung Hee-lee |
| Correspondent | Milan George Dio Medical Corporation 8770 W Bryn Mawr Ave. Ste. 1250 Chicago, IL 60631 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-29 |
| Decision Date | 2017-11-30 |
| Summary: | summary |