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Jazz Cap SP - one level

Jazz Cap SP

Cementless screw augmentation

CE
510(k)
  • Cementless pedicle screw augmentation
  • Adapted to poor quality spinal bone
  • Protect proximal fixation levels
  • Smart & fast locking mechanism

Innovative and unique concept addressing degenerative spine conditions, Jazz™ Cap SP (Screw Protection)  is the only band product that allows direct coupling with a pedicle screw (Jazz™ Screw). This screw supplementation significantly increases primary stability in situations of poor bone quality. 

Innovative and unique concept in the market addressing degenerative spine surgeons concerns, Jazz™ Cap SP (Screw Protection) is the only current solution that allows direct coupling with a pedicle screw (Jazz™ Screw) to supplement it. Significantly increase its primary stability in situations of poor quality of the patient’s bone
 

Jazz™ Cap SP allows you to create up to 4 fixation points on the same vertebra with minimal profile and that no other implant on the market can provide:

  • The pedicle fixation is ensured by the Jazz™ screw, whose surgical technique is standard
  • Sub-laminar fixation is allowed by the Jazz™ Cap SP, which is very quick to implement because it is easy and requires few instruments.

Supplied sterile, Jazz™ Cap SP is a real alternative to fenestrated screws using surgical cement or expansion screws, avoiding the numerous per and postoperative complications related to the recovery of these implants, found in the literature.

Thanks to its innovative screw and tape locking mechanisms and its modularity that automatically positions the belt in an optimal position just above the blade, Jazz™ Cap SP is characterized by its quick and easy implementation with a minimal learning curve.

Range

One unique implant.

Materials

Connector Locking Mechanism Band Buckle Metal Strip
Materials  Titanium alloy Ti6Al4V PEEK (PolyEtherEtherKetone) Optima LT1 Polyester Stainless steel Grade : 316L Stainless steel Grade : 304L/304
Standards   ISO 5832-3 ASTM F2026 / ASTM F139 ASTM F899 / ASTM A240

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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.