Kyphoplasty systems
Vertecem II Cement Kit
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 Vertecem II Cement Kit
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.
Vertecem II Cement Kit 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 |
|---|---|---|---|
| 08.702.017S | Weight 22 g | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Vertecem II Cement Kit 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 Vertecem II Cement Kit?
Vertecem II Cement Kit is made by OSARTIS GmbH. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Vertecem II Cement Kit come in?
Sizes listed for Vertecem II Cement Kit: Weight: 22 g. Confirm availability with the manufacturer's instructions for use.
Is Vertecem II Cement Kit MRI safe?
The FDA device database entry for Vertecem II Cement Kit does not state its MRI safety status. Check the labeling before MRI.
Is Vertecem II Cement Kit FDA cleared?
Vertecem II Cement Kit 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.