Kyphoplasty systems
BonOs Inject
by OSARTIS GmbH
A sterile substance intended to be used to replace cortical/cancellous bone in a vertebral body to stabilize vertebral compression fractures (VCFs) caused by cancer, osteoporosis, or trauma. The device may be a sterile powder of a synthetic polymer [e.g., polymethylmethacrylate (PMMA)] that is mixed with its sterile diluent, or a non-PMMA-containing elastomer formed by mixing two precursors, prior to implantation typically during a balloon kyphoplasty or vertebroplasty procedure. This device does not contain an antibiotic agent. After application, this device cannot be reused.
Where to buy BonOs Inject
We do not have contact details for OSARTIS GmbH yet. Send a request and we will route it to the right person for your country.
BonOs Inject 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 |
|---|---|---|---|
| 01-0309 | Weight 24 g | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is BonOs Inject used for?
A sterile substance intended to be used to replace cortical/cancellous bone in a vertebral body to stabilize vertebral compression fractures (VCFs) caused by cancer, osteoporosis, or trauma. The device may be a sterile powder of a synthetic polymer [e.g., polymethylmethacrylate (PMMA)] that is mixed with its sterile diluent, or a non-PMMA-containing elastomer formed by mixing two precursors, prior to implantation typically during a balloon kyphoplasty or vertebroplasty procedure. This device does not contain an antibiotic agent. After application, this device cannot be reused.
Who makes BonOs Inject?
BonOs Inject is made by OSARTIS GmbH. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does BonOs Inject come in?
Sizes listed for BonOs Inject: Weight: 24 g. Confirm availability with the manufacturer's instructions for use.
Is BonOs Inject MRI safe?
The FDA device database entry for BonOs Inject does not state its MRI safety status. Check the labeling before MRI.
Is BonOs Inject FDA cleared?
BonOs Inject is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a OSARTIS GmbH sales representative?
OSARTIS GmbH has not listed representatives on LA Vascular yet. Visit the OSARTIS GmbH 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.