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 |