Kyphoplasty systems
Cross-Fuse PEEK VBR/IBF System
by Pioneer Surgical Technology, 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 Cross-Fuse PEEK VBR/IBF System
We do not have contact details for Pioneer Surgical Technology, Inc. yet. Send a request and we will route it to the right person for your country.
Cross-Fuse PEEK VBR/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 |
|---|---|---|---|
| 35-TAMP | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Cross-Fuse PEEK VBR/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 Cross-Fuse PEEK VBR/IBF System?
Cross-Fuse PEEK VBR/IBF System is made by Pioneer Surgical Technology, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Cross-Fuse PEEK VBR/IBF System come in?
The FDA device database does not list sizes for Cross-Fuse PEEK VBR/IBF System. Check the instructions for use or ask a Pioneer Surgical Technology, Inc. representative.
Is Cross-Fuse PEEK VBR/IBF System MRI safe?
The FDA device database entry for Cross-Fuse PEEK VBR/IBF System does not state its MRI safety status. Check the labeling before MRI.
Is Cross-Fuse PEEK VBR/IBF System FDA cleared?
Cross-Fuse PEEK VBR/IBF System is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Pioneer Surgical Technology, Inc. sales representative?
Pioneer Surgical Technology, Inc. has not listed representatives on LA Vascular yet. Visit the Pioneer Surgical Technology, 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.