Kyphoplasty systems
VertebraLINK
A hand-held, surgical instrument designed to be used to manually pack tissue or other material during a surgical intervention. It typically consists of a shaft that terminates in a blunt (flat or profiled) tip at the distal end and a handle at the proximal end. It is typically a one-piece instrument made of metal, however some types may employ a synthetic material for the handle (e.g., Tufnol). The surgeon may pack the material by applying hand pressure to the device or by tapping the proximal end with a hammer/mallet. This is a reusable device.
Where to buy VertebraLINK
We do not have contact details for Linkspine, Inc. yet. Send a request and we will route it to the right person for your country.
VertebraLINK 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 |
|---|---|---|---|
| 84-0501/00 | — | Not stated | Available |
| 84-0501/50 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is VertebraLINK used for?
A hand-held, surgical instrument designed to be used to manually pack tissue or other material during a surgical intervention. It typically consists of a shaft that terminates in a blunt (flat or profiled) tip at the distal end and a handle at the proximal end. It is typically a one-piece instrument made of metal, however some types may employ a synthetic material for the handle (e.g., Tufnol). The surgeon may pack the material by applying hand pressure to the device or by tapping the proximal end with a hammer/mallet. This is a reusable device.
Who makes VertebraLINK?
VertebraLINK is made by Linkspine, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does VertebraLINK come in?
The FDA device database does not list sizes for VertebraLINK. Check the instructions for use or ask a Linkspine, Inc. representative.
Is VertebraLINK MRI safe?
The FDA device database entry for VertebraLINK does not state its MRI safety status. Check the labeling before MRI.
Is VertebraLINK FDA cleared?
VertebraLINK is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Linkspine, Inc. sales representative?
Linkspine, Inc. has not listed representatives on LA Vascular yet. Visit the Linkspine, 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.