The following data is part of a premarket notification filed by Huvexel Co., Ltd with the FDA for Rexious Spinal Fixation System.
| Device ID | K173131 | 
| 510k Number | K173131 | 
| Device Name: | Rexious Spinal Fixation System | 
| Classification | Thoracolumbosacral Pedicle Screw System | 
| 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 | NKB | 
| CFR Regulation Number | 888.3070 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Special | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2017-09-29 | 
| Decision Date | 2017-12-08 | 
| Summary: | summary |