Modification to Global Spinal Fixation System
FDA 510(k) K042928 · U&I Corp.
510(k) numberK042928
Submission
- Device name
- Modification to Global Spinal Fixation System
- Applicant
- U&I Corp.
Uijungbu, Gyeonggi-Do, KR - Received
- October 22, 2004
- Decision date
- February 17, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MNH – Orthosis, Spondylolisthesis Spinal Fixation
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3070
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code MNH
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K162066 | Reliance Spinal Screw SystemMNH · Traditional | Reliance Medical Systems, LLC | 12/02/2016SE |
| K162801 | CastleLoc Spinal Fixation SystemMNH · Special | L&K BIOMED Co., Ltd. | 11/03/2016SE |
| K162143 | FixxSure® X-LinkMNH · Traditional | Innovasis, Inc. | 09/23/2016SE |
| K161151 | Spinal fixation systemMNH · Traditional | Canwell Medical Co., Ltd. | 09/21/2016SE |
| K162189 | ANAX 5.5 Spinal SystemMNH · Special | U&I Corporation | 08/30/2016SE |
| K151362 | HC Spinal SystemMNH · Traditional | Hung Chun Bio-S Co., Ltd. | 05/05/2016SE |
| K153404 | Zavation Spinal SystemMNH · Traditional | Zavation, LLC | 04/21/2016SE |
| K160020 | Captiva Spine and CapLOX II/TowerLOX Pedicle Screw SystemMNH · Special | Captiva Spine | 03/02/2016SE |
| K143013 | Spinal Inner Fixation SystemMNH · Traditional | Changzhou Dingjian Medical Appliance Co., Ltd. | 12/11/2015SE |
| K151695 | Romeo posterior osteosynthesis systemMNH · Traditional | Spineart | 09/10/2015SE |
More from Spineart
| 510(k) | Device | Decision |
|---|---|---|
| K220147 | Aspiron S ACP SystemKWQ · Special | 02/16/2022SE |
| K210573 | Velofix SA Cervical CageOVE · Traditional | 11/19/2021SE |
| K183243 | Velofix TLIF CageMAX · Special | 07/10/2019SE |
| K190067 | Velofix Interbody Fusion SystemODP · Special | 02/04/2019SE |
| K190053 | SECULOK ACP SystemKWQ · Special | 02/01/2019SE |
| K181824 | CBT Screw Fixation SystemNKB · Traditional | 12/13/2018SE |
| K183383 | ANAX OCT Spinal SystemNKG · Special | 12/12/2018SE |
| K181829 | Velofix TLIF CageMAX · Special | 11/14/2018SE |
| K182055 | SECULOK ACP SystemKWQ · Traditional | 09/10/2018SE |
| K180759 | SECULOK Suture AnchorMBI · Traditional | 08/09/2018SE |
Questions and answers
When was Modification to Global Spinal Fixation System cleared by the FDA?
Modification to Global Spinal Fixation System (K042928) received a 510(k) decision of Substantially Equivalent on February 17, 2005, 118 days after the submission was received.
What is the product code of K042928?
The FDA product code is MNH – Orthosis, Spondylolisthesis Spinal Fixation, a Class II (moderate risk) device regulated under 21 CFR 888.3070.