Kyphoplasty systems
Vault C ACDF System
A collection of various orthopaedic surgical instruments, dressings and the necessary materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a reusable device.
Where to buy Vault C ACDF System
We do not have contact details for Precision Spine, Inc. yet. Send a request and we will route it to the right person for your country.
Vault C ACDF 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 |
|---|---|---|---|
| 37-IN-0050 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Vault C ACDF System used for?
A collection of various orthopaedic surgical instruments, dressings and the necessary materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a reusable device.
Who makes Vault C ACDF System?
Vault C ACDF System is made by Precision Spine, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Vault C ACDF System come in?
The FDA device database does not list sizes for Vault C ACDF System. Check the instructions for use or ask a Precision Spine, Inc. representative.
Is Vault C ACDF System MRI safe?
The FDA device database entry for Vault C ACDF System does not state its MRI safety status. Check the labeling before MRI.
Is Vault C ACDF System FDA cleared?
Vault C ACDF System is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Precision Spine, Inc. sales representative?
Precision Spine, Inc. has not listed representatives on LA Vascular yet. Visit the Precision Spine, Inc. 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.