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Jazz Lock & Jazz Band

Jazz Lock

Multipurpose fixation

CE
510(k)
  • Rodless band fixation
  • Smart fast locking mechanism
  • Single implant size with limited instrumentation
  • Ultra low profile
  • Sterile implants

The Jazz™ Lock system is based on the concept of spinal disorders treatment with band (braid) technology, expertise area of Implanet.

Traumatology Spine surgery with fixation sublaminar, interspinous or acticulars

Deformity spine correction.

Degenerative spine fusion to enhance screw fixation or as an alternative to a screw.

This expertise leads us to propose a new single implant for cerclage of the cervical levels, independently of any posterior fixation system, complementing the existing Jazz™ range.
With this unique new strapping system on the market, Implanet offers a credible and efficient alternative, addressing the problems encountered with the metal cable systems.

  • Unique concept on the market
  • French design and manufacturing, complying with Directive 93/42/EC
  • Connector for independent locking band for later treatment of cervical levels
  • Bone/implant interface: braided belt fits the anatomical structures
  • Simple and rapid implementation
  • Open and flat polyester Band coming from the Jazz™ Platform: Proven concept
  • No metal in the canal = no artifact
  • Single tensioning instrument for reduction and correction of the spine based on
  • Jazz™ PlatformOptimal instrumentation only made of 4 instruments, with 3 common to the Jazz™ Platform
  • Limited learning curve due to the simplicity of the implant and instrumentation solution

Range

One unique implant, adaptable to any spine anatomies with a posterior approach.

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
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.

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