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Jazz Frame

Jazz Frame

Posterior Fixation

CE
510(k)
  • Correction by Frame Technique
  • Suitable for 5.5 and 6.0mm rods

Jazz™Frame T-Bar implants associated to the sublaminar Jazz™ solution are used to create an extremely rigid frame which is sufficient to obtain a postero-medial translation necessary in the scoliosis treatment. This translation is impossible to obtain with screws.

Jazz™Frame T-Bar implants associated to the sublaminar Jazz™ solution are used to create an extremely rigid frame which is sufficient to obtain a postero-medial translation necessary in the scoliosis treatment. This translation is impossible to obtain with screws.

This technique, named the Frame Technique, consists in assembling Jazz™ Frame T-Bar connectors positioned at the top and at the apex and two similar bended rods. This assembled frame is used to obtain a correction of the spine in the sagittal plan. This very rigid frame is used to tension the spine and makes it approach the frame and, at the contrary, prevents the frame itself to approach the spine.

The rigidity of the frame and the tensioned sublaminar Jazz™ connected to it, respect the sagittal curve and the frontal alignment determined by the physician. This construct realizes, automatically, most of or all the derotation given to the spine. For more information, refer to the Jazz™ Surgical technique.

This technique has been the subject of many national and international publications with remarkable clinical results.

This technique allows significant reductions of:

  • operating times
  • co-morbidities in particular regarding the blood loss
  • the total number of implants required
  • X-ray doses administered to patients, due to the use of Jazz™, reducing the number of pedicle screws
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Jazz Frame

In terms of technical characteristics of the implant, note:

  • fixed closed transverse connectors can be used with 5.5 or 6.0 mm in diameter rods and support the very high mechanical stresses applied to the construct
  • Simple and rapid implementation without learning curve
  • Sterile Implant
  • Only use of the screwdriver 3.5 mm already in instrumentation. No specific instrument
  • French design and manufacturing, in compliance with Directive 93/42 / EC

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

For Rod Diameters (mm) Length
5.5 / 6.0 25
5.5 / 6.0 30
5.5 / 6.0 35

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Implanet
Les dispositifs médicaux classe IIb d’Implanet sont marqués CE 0459 avec le GMED selon la Directive 93/42/CEE et ses amendements.
Avant toute utilisation d’un produit, veuillez-vous référer à la notice d’instructions et à la technique opératoire. Consulter la notice du produit pour la liste complète des indications, contre-indications, mises en garde et précautions d’emploi. 
Statut du remboursement en France : les implants sont inscrits à la Liste des Produits et Prestations Remboursables (LPPR) mentionnée à l’article L165-1 du code de la sécurité sociale et sont, de ce fait, éligibles au remboursement par l’assurance maladie.

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.