Kyphoplasty systems

StabiliT ER2 Bone Cement

by Dfine, Inc.

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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StabiliT ER2 Bone Cement models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
1135— Not statedAvailable

Procedures that use kyphoplasty systems

Frequently asked questions

What is StabiliT ER2 Bone Cement 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 StabiliT ER2 Bone Cement?

StabiliT ER2 Bone Cement is made by Dfine, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.

What sizes does StabiliT ER2 Bone Cement come in?

The FDA device database does not list sizes for StabiliT ER2 Bone Cement. Check the instructions for use or ask a Dfine, Inc. representative.

Is StabiliT ER2 Bone Cement MRI safe?

The FDA device database entry for StabiliT ER2 Bone Cement does not state its MRI safety status. Check the labeling before MRI.

Is StabiliT ER2 Bone Cement FDA cleared?

StabiliT ER2 Bone Cement is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Dfine, Inc. sales representative?

Dfine, Inc. has not listed representatives on LA Vascular yet. Visit the Dfine, 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.

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