Vertebral Body Augmentation System
TRIPOD-FIX Vertebral Body Augmentation System is designed for the treatment of vertebral compression fractures (VCFs), and it is intended to be used with polymethylmethacrylate (PMMA) bone cement for percataneous vertebral augmentation.
The system consists of an implantable expandion stant and associated surgical instruments. The stent is inserted into the collapsed vertebral body, by following transpedicular approach and expanded mechanically to restore the anatomical height. Three-dimension expansion machanism provides the solid support of vertebral height restoration.
Indication
TRIPOD-FIX
TRIPOD-FIX Vertebral Body Augmentation System is indicated for use in the reduction of painful osteoporotic vertebral compression fractures. It is intended to be used in combination with polymethylmethacrylate (PMMA) bone cement during percutaneous vertebral augmentation surgery.
Feature & Benefit
TRIPOD-FIX Vertebral Body Augmentation System
Tripod-Fix after expansion
Provides anatomical restorationand controllable implant expansion during a procedure for treating VCF, especially wedge fracture.
Three-dimensional expansion provides stable support.
Three-dimension expansion mechanism allows the fuller distribution of bone cement to provide stable maintenance of restoration.
Implant placement
three-dimensional expansion
Bone cement injection
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Product Specification
TRIPOD-FIX 5.0 System & 5.8 System
REF No.
40-465000
40-465800
Material
Ti-6Al-4V ELI
Ti-6Al-4V ELI
Color
Gold
Dark blue
Unexpanded Diameter
5.0 mm
5.8 mm
Length
25.0 mm
28.0 mm
Full Expansion Height
15.0 mm
17.0 mm
Minimum Pedicle Channel Diameter
5.7 mm
6.5 mm
Instrumente für Expansionsstent 5.0 System & 5.8 System
Preparation and Implant Placement
85035
85036
Driver
70125
70125
Guide Wire
85016
85006
Working Cannula
85013
85004
Drill
85029
85030
Cannula Plug
85017
85008
Reamer
85009
85009
Detacher
Instruments for Expansion Stent
Bone Cement Injection
85010
Cement Pusher
85011
Cement Transfer Tube
Risks and contraindications
Like all surgical procedures, kyphoplasty using an intravertebral instrumental vertebral body realignment system carries risks, including serious complications, and the procedure is not suitable for all patients. Comprehensive information on risks, contraindications, warnings and precautions can be found in the instructions for use of the system. Before use, please read the instructions for use for indications, contraindications, warnings, precautions and instructions for use.
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