A full family of VCF solutions to match the unique needs of every patient.

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The StabiliT System combines a targeted approach and ultra-high viscosity cement to repair compression fractures and minimize extravasation in the vertebrae.

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StabiliT MX provides a targeted, bone-sparing cavity creation approach to vertebral augmentation with DFINE’s patented cement preparation and controlled delivery of high-viscosity cement.

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StabiliT VP combines DFINE’s patented simple cement preparation with the controlled delivery of high-viscosity cement.

 

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  • “The Osteotome was designed to articulate and bend to create multiple pathways for the cement without damage to the healthy bone. The robustness within the system to make a curve within a bone is absolutely remarkable.”

    James Carlisle, M.D.
    Utah Vascular Imaging Salt Lake City, Utah

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Combines a targeted approach and ultra-high viscosity cement to repair compression fractures and minimize extravasation in the vertebrae.

Minimizes Extravasation

Preferential cavity creation, controlled delivery, and consistent RF modulated ultra-high viscosity bone cement help minimize the potential for extravasation.1

Minimized extravasation 2

Maximizes Interdigitation

The articulating MidLine Osteotome minimizes the destruction of intact cancellous bone and maximizes interdigitation for optimally filled and mechanically sound vertebrae.2

Reduces Exposure

The StabiliT system allows users to stand up to 20 feet away from x-ray sources and reduce radiation exposure.

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StabiliT System Overview

Radiographic example of VertecoR MidLine Osteotome in use.

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A targeted, bone-sparing approach to vertebral augmentation with DFINE’s patented cement preparation and controlled delivery of high-viscosity cement.

Targeted Cavity Creation

  • Enables targeted cavity creation across the vertebral midline (unipedicular access)
  • Spares healthy cancellous bone
  • Maximizes exposed surface area to facilitate interdigitation
  • Lessens the impact of fracture morphology on cement distribution by creating preferential pathways

High Viscosity Cement

  • Simple, patented vacuum cement mixing system
  • Extended working time; 35 minutes for procedural flexibility
  • Barium sulfate radiopacifier

Excellent Control

  • Precise cement delivery and stoppage for predictable results
  • Reduced radiation exposure with 24-inch delivery line
  • “The StabiliT system provides very high viscosity cement and long working time. This allows us to go slowly and carefully getting the best cement fill possible in each vertebra and if needed treat more than one level. The Osteotome allows us to access in a unipediculate manner and still reach across the entire vertebrae to make the pathways for the cement.”

    Bassem Georgy
    Interventional Neuroradiologist San Diego Imaging | Escondido, CA
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The StabiliT VP Vertebroplasty System combines DFINE’s patented simple cement preparation with the controlled delivery of high-viscosity cement.

Simplicity

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Simple cement preparation

  • No blending, shaking, squeezing, or stirring
  • Mixing cartridge used for delivery; no need to transfer cement

Speed

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Superior cement viscosity and working time

  • Up to 2x viscosity of standard PMMA cements*; designed for consistent filling and interdigitation
  • Extended working time >30 minutes for procedural flexibility*
  • Barium sulfate radiopacifier for excellent visibility

Control

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Controlled delivery

  • Precise cement delivery and stoppage for predictable results
  • Reduced radiation exposure with 24-inch delivery line

* Tests performed and data on file at DFINE, Inc.

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Indications for Use

 

StabiliT® Vertebral Augmentation System

The StabiliT® Vertebral Augmentation System is intended for percutaneous delivery of StabiliT® ER2 Bone Cement. The StabiliT® ER2 Bone Cement is indicated for the treatment of pathological fractures of the vertebrae using a vertebroplasty or kyphoplasty procedure. Painful vertebral compression fractures may result from osteoporosis, benign lesions (hemangioma), and malignant lesions (metastatic cancers, myeloma).

StabiliT® MX Vertebral Augmentation System

The StabiliT® MX Vertebral Augmentation System is intended for percutaneous delivery of StabiliT® Bone Cement. The StabiliT® Bone Cement is indicated for the treatment of pathological fractures of the vertebrae using a vertebroplasty or kyphoplasty procedure. Painful vertebral compression fractures may result from osteoporosis, benign lesions (hemangioma), and malignant lesions (metastatic cancers, myeloma).

StabiliT® VP Vertebroplasty System

The StabiliT® VP Vertebroplasty System is intended for percutaneous delivery of StabiliT® Bone Cement. The StabiliT® Bone Cement is indicated for the treatment of pathological fractures of the vertebrae using a vertebroplasty or kyphoplasty procedure. Painful vertebral compression fractures may result from osteoporosis, benign lesions (hemangioma), and malignant lesions (metastatic cancers, myeloma).

 

Risks and Contraindications

As with most surgical procedures, there are risks associated with the StabiliT® procedure, including serious complications. For complete information regarding risks, contraindications, warnings, and precautions, please review the systems’ Instruction for Use. For more information regarding bone cement adverse events, please see our Indications Page.  For complete information regarding System related adverse events please see Instructions for Use.