Kyphoplasty systems
Fortilink-C IBF System
by Xtant Medical Holdings, Inc.
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 Fortilink-C IBF System
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Fortilink-C IBF 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 |
|---|---|---|---|
| 65-C-Tamp-LG | — | Not stated | Available |
| 65-C-Tamp-SM | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Fortilink-C IBF System 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 Fortilink-C IBF System?
Fortilink-C IBF System is made by Xtant Medical Holdings, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Fortilink-C IBF System come in?
The FDA device database does not list sizes for Fortilink-C IBF System. Check the instructions for use or ask a Xtant Medical Holdings, Inc. representative.
Is Fortilink-C IBF System MRI safe?
The FDA device database entry for Fortilink-C IBF System does not state its MRI safety status. Check the labeling before MRI.
Is Fortilink-C IBF System FDA cleared?
Fortilink-C IBF System is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Xtant Medical Holdings, Inc. sales representative?
Xtant Medical Holdings, Inc. has not listed representatives on LA Vascular yet. Visit the Xtant Medical Holdings, 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.