Kyphoplasty systems
Osteoflex
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.
Where to buy Osteoflex
We do not have contact details for Pan Medical US Corporation yet. Send a request and we will route it to the right person for your country.
Osteoflex 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 |
|---|---|---|---|
| INTV-CEM | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Osteoflex 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 Osteoflex?
Osteoflex is made by Pan Medical US Corporation. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Osteoflex come in?
The FDA device database does not list sizes for Osteoflex. Check the instructions for use or ask a Pan Medical US Corporation representative.
Is Osteoflex MRI safe?
The FDA device database entry for Osteoflex does not state its MRI safety status. Check the labeling before MRI.
Is Osteoflex FDA cleared?
Osteoflex is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Pan Medical US Corporation sales representative?
Pan Medical US Corporation has not listed representatives on LA Vascular yet. Visit the Pan Medical US 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.