Kyphoplasty systems
VEO Lateral Interbody Fusion System
A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.
Where to buy VEO Lateral Interbody Fusion System
We do not have contact details for Choice Spine, LP yet. Send a request and we will route it to the right person for your country.
VEO Lateral Interbody Fusion System models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 20-3006 | — | Not stated | Available |
| V070-0110 | — | Not stated | Available |
FDA clearances
- 510(k) K123997 April 2013
Procedures that use kyphoplasty systems
Frequently asked questions
What is VEO Lateral Interbody Fusion System used for?
A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.
Who makes VEO Lateral Interbody Fusion System?
VEO Lateral Interbody Fusion System is made by Choice Spine, LP. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does VEO Lateral Interbody Fusion System come in?
The FDA device database does not list sizes for VEO Lateral Interbody Fusion System. Check the instructions for use or ask a Choice Spine, LP representative.
Is VEO Lateral Interbody Fusion System MRI safe?
The FDA device database entry for VEO Lateral Interbody Fusion System does not state its MRI safety status. Check the labeling before MRI.
Is VEO Lateral Interbody Fusion System FDA cleared?
VEO Lateral Interbody Fusion System is covered by FDA submission K123997.
How do I contact a Choice Spine, LP sales representative?
Choice Spine, LP has not listed representatives on LA Vascular yet. Visit the Choice Spine, LP company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.