Kyphoplasty systems
Vertefix
A substance designed to be used in arthroplastic and/or osteosynthetic procedures for the fixation of polymer or metallic implants to the living bone. It may also be intended for use as a filler in the case of bone pathologies (e.g., to stabilize and reinforce vertebral body structures in vertebroplasty and kyphoplasty). It is typically made from methylmethacrylate, polymethylmethacrylate (PMMA), esters of methacrylic acid or copolymers containing polymethylmethacrylate and polystyrene. This device does not contain an antimicrobial agent. After application, this device cannot be reused.
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Where to buy Vertefix
Contact Cook Incorporated directly; they can quote, ship, or point you to the distributor for your country.
From cookmedical.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.
Procedures that use kyphoplasty systems
Frequently asked questions
What is Vertefix used for?
A substance designed to be used in arthroplastic and/or osteosynthetic procedures for the fixation of polymer or metallic implants to the living bone. It may also be intended for use as a filler in the case of bone pathologies (e.g., to stabilize and reinforce vertebral body structures in vertebroplasty and kyphoplasty). It is typically made from methylmethacrylate, polymethylmethacrylate (PMMA), esters of methacrylic acid or copolymers containing polymethylmethacrylate and polystyrene. This device does not contain an antimicrobial agent. After application, this device cannot be reused.
Who makes Vertefix?
Vertefix is made by Cook Incorporated. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Vertefix come in?
The FDA device database does not list sizes for Vertefix. Check the instructions for use or ask a Cook Incorporated representative.
Is Vertefix MRI safe?
The FDA device database entry for Vertefix does not state its MRI safety status. Check the labeling before MRI.
Is Vertefix FDA cleared?
Vertefix is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Cook Incorporated sales representative?
Cook Incorporated has not listed representatives on LA Vascular yet. Visit the Cook Incorporated 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.