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Jazz ™ Evo
Our reference in scoliosis treatment
CE
510(k)
- For use with all vertebral structures
- Fixation regardless of bone quality
- Most complete product range on the market
- Sterile implants
The Jazz™ Evo system offers the most complete range of connectors on the market, for fixation around all vertebral structures.
A true three-dimensional correction
Combined with its simple and powerful tensioner,
Jazz™ Evo allows postero-medial translation...
... as well as derotation, in particular by detorsion of the spine.
Restoration of the sagittal plane, avoids the risk of a flat back:
Offers the practitioner spine correction possibilities, regardless of bone quality. The width of the band induces a reduction in the mechanical stresses on the bone.
Reduced stress on the bone and fixation regardless of bone quality.
Jazz™ Evo is based on union rods alloy made of titanium (Ti6Al4V) or cobalt-chrome (CoCr).
- Jazz™ Evo is designed for multiple union rod diameters: 3.5 – 4.0 – 4.5 – 4.75 – 5.0 – 5.5 – 6.0 mm
- Unique implant: one size fits all levels
- Primary stability on the rod: auto-stable / snap-on implant
- Bone / implant interface: adapting and strapping the anatomical structures thanks to the braid
- 2-in-1 rod and braid locking mechanism
- Open flat polyester braid
- Per-operative and post-operative intra-canalar follow-up: No metal part in the canal => no artifacts thanks to the braid
- Single tensioning instrument for reduction and correction of the spine
- 4-in-1 instrumentation for stabilization, snapping, unsnapping and counter-torquing/anti-rotation of the implant during final tightening
Materials
| Connector & screw | Band | Buckle | Metal Strip | |
|---|---|---|---|---|
| Materials | Titanium alloy Ti6Al4V | Polyester | Stainless steel Grade : 316L | Stainless steel Grade : 304L/304 |
| Standards | ISO 5832-3 | / | ASTM F139 | ASTM F899 / ASTM A240 |
Range
| Rod diameter | 3.5 | 4.0 | 4.5 | 4.75 | 5.0 | 5.5 | 6.0 | 6.35* |
|---|---|---|---|---|---|---|---|---|
| Availability | x | x | x | x | x | x | x | x |
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Implanet
Class IIb medical devices of Implanet are CE 0459 marked with GMED, according to Directive 93/42/EEC and its amendments.
Before using a product, please refer to the instructions for use and the operative technique. Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.
Before using a product, please refer to the instructions for use and the operative technique. Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.
Class II medical devices of Implanet are 510(k) cleared.
Federal Law restricts this device to sale by or on the order of a physician.
Before using a product, please refer to the instructions for use and the operative/surgical technique.
Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.va
Federal Law restricts this device to sale by or on the order of a physician.
Before using a product, please refer to the instructions for use and the operative/surgical technique.
Consult instructions for use for a complete list of indications, contraindications, warnings and precautions for use.va
