Kyphoplasty systems
PILLAR SA Ti
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 PILLAR SA Ti
We do not have contact details for Orthofix US LLC yet. Send a request and we will route it to the right person for your country.
PILLAR SA Ti 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 |
|---|---|---|---|
| 82-1001 | — | Not stated | Available |
| 82-1002 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is PILLAR SA Ti 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 PILLAR SA Ti?
PILLAR SA Ti is made by Orthofix US LLC. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does PILLAR SA Ti come in?
The FDA device database does not list sizes for PILLAR SA Ti. Check the instructions for use or ask a Orthofix US LLC representative.
Is PILLAR SA Ti MRI safe?
The FDA device database entry for PILLAR SA Ti does not state its MRI safety status. Check the labeling before MRI.
Is PILLAR SA Ti FDA cleared?
PILLAR SA Ti is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Orthofix US LLC sales representative?
Orthofix US LLC has not listed representatives on LA Vascular yet. Visit the Orthofix US LLC 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.