MIS Solutions

Zimmer Biomet Spine is committed to advancing and developing ground-breaking solutions for differentiated complex and minimally-invasive (MIS) spine procedures. Our MIS systems, including our Vital™ MIS Spinal Fixation System and Alpine XCAdjustable Fusion System, are backed by a legacy of clinical success and offer enhanced procedural freedom and streamlined workflow for spine surgeons and hospitals. Zimmer Biomet Spine is committed to delivering less invasive solutions through intuitive and versatile implants and instrumentation.

Motion Preservation

Zimmer Biomet Spine’s cervical arthroplasty device, the Mobi-C® Cervical Disc (Mobi-C), is the first cervical disc replacement FDA approved for both one and two-level indications. Designed to restore segmental motion and disc height, Mobi-C was approved after an extensive Investigational Device Exemption (IDE) study. In the two-level arm of the IDE, Mobi-C demonstrated superiority in overall trial success compared to fusion at 84 months.  Zimmer Biomet Spine is committed to advancing cervical arthroplasty as the standard of care in indicated patients.

Cervical Solutions

Zimmer Biomet Spine utilizes its deep industry knowledge and expertise to refine a comprehensive anterior cervical product portfolio of next generation devices that includes Trabecular Metal Technology, PEEK and allograft options. Our implants are designed to facilitate efficient, versatile, and reproducible spinal fusion procedures ready to meet the needs of surgeons and their patients in an ever-changing global spine market. 

Anterior/Lateral Thoracolumbar Solutions

Zimmer Biomet Spine’s comprehensive thoracolumbar products are engineered to treat spinal deformities, degenerative, and complex cases with clinical effectiveness, always with a commitment to patient safety. Our lateral solutions include powerful tools like the Timberline® Lateral Fusion System, which offers a three-blade retractor, standard and hyperlordotic spacers, and modular plate/screw fixation options, allowing spine surgeons a wide variety of tools to improve patient outcomes.

Posterior Thoracolumbar Solutions

Zimmer Biomet Spine’s thoracolumbar products optimize performance during surgery while providing spine professionals a comprehensive product suite for long-term, one-stop solutions. The Tether –Vertebral Body Tethering System is the only FDA approved spinal tethering device used as an alternative to spinal fusion for children with Adolescent Idiopathic Scoliosis. The Tether is designed to allow the spine to bend and flex, rather than being fixed in place and uses the patient’s natural remaining growth to achieve correction of scoliosis overtime. The Vital™ / Vitality® Spinal Fixation System is an all-inclusive pedicle screw platform that provides surgeons with all of the vital components needed to execute rigid fixation of challenging anatomy in complex thoracolumbar spine procedures. And our wide range of interbody devices includes the TrellOss™ Porous Ti Systems, Trabecular Metal™ Material, and PEEK lumbar fusion options, with comprehensive instrumentation systems. 

Biologics Solutions

Zimmer Biomet Spine offers a full line of biologics products including advanced allografts, synthetic bone void fillers, and allograft demineralized bone matrix products to provide best-in-class biologic solutions for use in spine surgery. Our PrimaGen Advanced Allograft is a fresh frozen allograft that provides advanced bone healing support by preserving more of the native bone tissue in order to provide all three components of the bone healing triad.

All content herein is protected by copyright, trademarks and other intellectual property rights, as applicable, owned by or licensed to Zimmer Biomet or its affiliates unless otherwise indicated, and must not be redistributed, duplicated or disclosed, in whole or in part, without the express written consent of Zimmer Biomet. 

This material is intended for health care professionals. Distribution to any other recipient is prohibited.

For product information, including indications, contraindications, warnings, precautions, potential adverse effects and patient counseling information, see the package insert and information on this website. To obtain a copy of the current Instructions for Use (IFU) for full prescribing and risk information, please call 1-800-348-2759, press 4 for 411 Technical Support.