The following data is part of a premarket notification filed by U&i Corp. with the FDA for Modification To Global Spinal Fixation System.
Device ID | K042928 |
510k Number | K042928 |
Device Name: | MODIFICATION TO GLOBAL SPINAL FIXATION SYSTEM |
Classification | Orthosis, Spondylolisthesis Spinal Fixation |
Applicant | U&I CORP. 529-1 YONGHYUN-DONG Euijungbu, Kyunggi-do, KR 480-050 |
Contact | Betty Lim |
Correspondent | Betty Lim U&I CORP. 529-1 YONGHYUN-DONG Euijungbu, Kyunggi-do, KR 480-050 |
Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-10-22 |
Decision Date | 2005-02-17 |
Summary: | summary |