The JAZZ Posterior Fixation systems are temporary implants to be used in orthopedic surgery. The JAZZ systems are intended to provide temporary stabilization as a bone anchor during the development of solid bony fusion and aid in the repair of bone fractures.
The JAZZ systems are designed primarily for a posterior fixation. The indications for use include the following applications:
- Traumatic spinal surgery, use in sub-laminar and interspinous cases and in facet connection techniques
- Surgery for spinal deformations such as scoliosis, kyphosis, lordosis, etc.
- Degenerative spinal surgery as a supplement to vertebral fusion, such as degenerative discopathy, stenosis, or spondylisthesis.
The JAZZ Systems may also be used in conjunction with other medical implants made of titanium alloy or Cobalt-chromium-molybdenum alloy whenever “wiring” may help secure the attachment of other implants.
The Jazz Claw System (hooks and rods) is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion of the thoracic, lumbar and/or sacral spine. The Jazz Claw System (hooks and rods) is intended for posterior fixation for the following indications: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, spinal deformities (i.e., scoliosis, kyphosis and/or lordosis), tumor, pseudarthrosis or revision of a failed fusion attempt.
The Jazz Claw System (hooks and rods) is indicated as an adjunct to fusion to treat adolescent idiopathic scoliosis. These devices are to be used with autograft and/or allograft.
Benefits:
- French design and manufacturing, in compliance with Directive 93/42/EC.
- Sterile implant.
- JAZZTM Band is designed for multiple union rod diameters: 3.5-4.5-4.75-5.5-6.0 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.
- Optimized instrumentation only made of 6 types of instruments : reduces the number of surgical steps, simple, effective and easy to use.
- Reduced co-morbidity and bleeding compared to pedicle screws.
- Operative technique less risky than pedicle screw fixation
Product Brochure: Jazz Product and Surgical Technique Brochure
About Spinal Fixation Band
It is a temporary orthopedic implant intended to provide stabilization during the development of solid bony fusion and aid in the repair of bone fractures. The indications for use include the following applications: 1 . Spinal trauma surgery, used in sublaminar or facet wiring techniques; 2. Spinal reconstructive surgery, incorporated into constructs for the purpose of correction of spinal deformities such as idiopathic and neuromuscular scoliosis in patients 8 years of age and older, adult scoliosis, kyphosis, and spondylolisthesis; 3. Spinal degenerative surgery, as an adjunct to spinal fusions.The device system is designed to be incorporated into constructs and used in conjunction with other medical device implants made of either stainless steel or titanium whenever “wiring’ may help secure the attachment of other implants.It stabilizes the spine as an adjunct to fusion in the correction of spinal deformities.
About Implanet
Implanet focuses on spine and knee products.
Its flagship product, the JAZZ™ Band latest generation implant, is intended to improve the treatment of spinal disorders requiring spinal fusion surgery. Protected by 4 sets of international patents, JAZZ has obtained 510(k) clearance from the Food and Drug Administration (FDA) in the United States and the CE mark.
Taking into account the evolution of the global healthcare system, the Implanet Marketing team identifies a portfolio of products and services based on a detailed analysis of socio-economic, regulatory, demographic and cultural specifications. The Implanet R&D team focuses on a scientifically and clinically proven implant design, using top quality materials tested to the highest prevailing standards, associated with simple and user-friendly instrumentation.
Our various workgroups, composed of surgeons, experienced engineers and product managers work closely together to offer a range of implants with scientifically sound specifications and the highest quality to adequately respond to requirements of healthcare professionals.
Implanet is able to provide the best of what science and experience have to offer, while ensuring to the stakeholders the best value for their products, their needs and demands. https://www.implanet.com