Spineart Sa
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Contact: Franck Pennesi
Web: http://www.spineart.ch
E-Mail:
Address: 20 Route De Pre Bois, Cp 1813, Geneva 1215, Switzerland
Phone: +41-(22)-7994020 | Fax: +41-(22)-7994026 | Map/Directions >>
Contact: Franck Pennesi
Web: http://www.spineart.ch
E-Mail:
Address: 20 Route De Pre Bois, Cp 1813, Geneva 1215, Switzerland
Phone: +41-(22)-7994020 | Fax: +41-(22)-7994026 | Map/Directions >>
Profile: Spineart Sa designs and markets spine patented implants. We provide Baguera® C which is a cervical disc prosthesis that is pre-assembled, & MRI-compatible. Tryptik® CA cervical & Juliet® lumbar interbody cage are designed to accelerate and improve the fusion process. Yoda® interspinous device enables natural movement of the spine. Romeo® posterior fixation system is inserted into the pedicle to facilitate and increase the safety of the surgical procedure.
FDA Registration Number: 3007728266
US Agent: Jerome Trividic / Spineart Usa
Phone: +1-(949)-313-6400 Fax: +1-(646)-304-1001 E-Mail:
13 Products/Services (Click for related suppliers)
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| • Cervical Intervertebral Fusion Device With Bone Graft (FDA Code: ODP / 888.3080) |
| • Disc Prosthesis |
| • Fusion Posterior Metal/Polymer Spinal System (FDA Code: NQP / 888.3070) Pedicle screw spinal systems are multiple component devices, made from a variety of materials, including alloys such as 316L stainless steel, 316LVM stainless steel, 22Cr-13Ni-5Mn stainless steel, Ti-6Al-4V, and unalloyed titanium, that allow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. Such a spinal implant assembly consists of a combination of anchors (e.g., bolts, hooks, and/or screws); interconnection mechanisms incorporating nuts, screws, sleeves, or bolts; longitudinal members (e.g., plates, rods, and/or plate/rod combinations); and/or transverse connectors. |
| • Intersomatic Lumbar Cages |
| • Interspinous Process Distraction Device |
| • Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX / 888.3080) |
| • Spinal Fixation Device |
| • Spinal Interlaminal Fixation Appliance (FDA Code: KWP / 888.3050) A spinal interlaminal fixation orthosis is a device intended to be implanted made of an alloy, such as stainless steel, that consists of various hooks and a posteriorly placed compression or distraction rod. The device is implanted, usually across three adjacent vertebrae, to straighten and immobilize the spine to allow bone grafts to unite and fuse the vertebrae together. The device is used primarily in the treatment of scoliosis (a lateral curvature of the spine), but it also may be used in the treatment of fracture or dislocation of the spine, grades 3 and 4 of spondylolisthesis (a dislocation of the spinal column), and lower back syndrome. |
| • Spinal Motion Preservation System |
| • Spinal Pedicle Fixation Orthosis (FDA Code: MNI / 888.3070) |
| • Spinal Products |
| • Spine Implants |
| • Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH / 888.3070) |
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