Kyphoplasty systems
VertaPlex HV
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.
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Where to buy VertaPlex HV
Contact Stryker Corporation directly; they can quote, ship, or point you to the distributor for your country.
From stryker.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
VertaPlex HV 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 |
|---|---|---|---|
| 0406622015 | — | MR Safe | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is VertaPlex HV 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 VertaPlex HV?
VertaPlex HV is made by Stryker Corporation. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does VertaPlex HV come in?
The FDA device database does not list sizes for VertaPlex HV. Check the instructions for use or ask a Stryker Corporation representative.
Is VertaPlex HV MRI safe?
The FDA device database lists VertaPlex HV as MR Safe. Always follow the specific MRI conditions in the labeling.
Is VertaPlex HV FDA cleared?
VertaPlex HV is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Stryker Corporation sales representative?
Stryker Corporation has not listed representatives on LA Vascular yet. Visit the Stryker Corporation 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.