Profile: Calvary Spine, Llc offers interbody fusion devices which are manufactured from Peek-Optima® polymer. The fusion devices are used in the treatment of degenerative disc diseases to assist fusion and restore disc height. Our calvary spine products are lumbar and cervical inter-body fusion devices made with peek-Optima®. Our lumbar interbody fusion device features Peek-Optima polymer with proven long-term biocompatibility and a modulus of elasticity between cortical and cancellous bone, curved contour that facilitates placement at the periphery of the disk space for contact with the most dense endplate bone surface ridges that resist implant migration, while providing a broader surface area to prevent subsidence.
FDA Registration Number: 3007279845
7 Products/Services (Click for related suppliers)
|
• Cervical Inter-body Fusion Devices |
• Cervical Intervertebral Fusion Device With Bone Graft (FDA Code: ODP / 888.3080) |
• Lumbar |
• Lumbar Interbody Fusion Devices |
• Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX / 888.3080) |
• Spinal Pedicle Fixation Orthosis For Degenerative Disc Disease (FDA Code: NKB / 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. |
• Spinal Products |