Kyphoplasty systems
Multi System
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 Multi System
We do not have contact details for Paragon 28, Inc. yet. Send a request and we will route it to the right person for your country.
Multi 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 |
|---|---|---|---|
| P99-150-0002 | — | MR Unsafe | Available |
| P99-150-0003 | — | MR Unsafe | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Multi 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 Multi System?
Multi System is made by Paragon 28, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Multi System come in?
The FDA device database does not list sizes for Multi System. Check the instructions for use or ask a Paragon 28, Inc. representative.
Is Multi System MRI safe?
The FDA device database lists Multi System as MR Unsafe. Always follow the specific MRI conditions in the labeling.
Is Multi System FDA cleared?
Multi System is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Paragon 28, Inc. sales representative?
Paragon 28, Inc. has not listed representatives on LA Vascular yet. Visit the Paragon 28, 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.