Kyphoplasty systems
ShurFit MALIF System
A collection of various orthopaedic surgical instruments, dressings and the necessary materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a reusable device.
Where to buy ShurFit MALIF System
We do not have contact details for Precision Spine, Inc. yet. Send a request and we will route it to the right person for your country.
ShurFit MALIF 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 |
|---|---|---|---|
| 23-9038 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is ShurFit MALIF System used for?
A collection of various orthopaedic surgical instruments, dressings and the necessary materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a reusable device.
Who makes ShurFit MALIF System?
ShurFit MALIF System is made by Precision Spine, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does ShurFit MALIF System come in?
The FDA device database does not list sizes for ShurFit MALIF System. Check the instructions for use or ask a Precision Spine, Inc. representative.
Is ShurFit MALIF System MRI safe?
The FDA device database entry for ShurFit MALIF System does not state its MRI safety status. Check the labeling before MRI.
Is ShurFit MALIF System FDA cleared?
ShurFit MALIF System is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Precision Spine, Inc. sales representative?
Precision Spine, Inc. has not listed representatives on LA Vascular yet. Visit the Precision Spine, 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.