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Xpendriv Cage

August 5, 2018 By SPINEMarketGroup

Auxein Spine’s Xpendriv Cage Vertebral Body Replacement System is intended to replace a vertebral body or an entire vertebra. It is for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged or unstable vertebral body or vertebra resected or excised during total and partial corpectomy and vertebrectomy procedures due to tumor or trauma (i.e., fracture). The Xpendriv system is intended to be used with supplemental internal fixation. The supplemental internal fixation systems that may be used with Xpendriv include. The use of bone graft with the Xpendriv system is optional.

  • Xpendriv-Cage-System-Brochure.Auxein.pdf

Benefits:

  • The Xpendriv Cages are composed of titanium alloy.
  • Auxein Spine’s Xpendriv System is intended to replace a vertebral body or an entire vertebra.

About Expandable Corpectomy Devices

Each year, there are more than 150,000 spinal fractures in North America*.  There is an estimated 10,000 to 12,000 spinal cord injuries every year and approximately 39% of these injuries are cause by motor vehicle accidents4. These non-elective or trauma surgeries sometimes require additional spinal structural support which is when the Expandable Corpectomy Device are used.Another indication or use for these Devices is in the treatment of cancer patients. If the cancer metastasizes or spreads in the spine, the surgeon may opt to remove the affected vertebral bodies and replace them with an Expandable Corpectomy Device.*(http://emedicine.medscape.com/article/1264191-overview)

About Auxein

At Auxein Medical we work with a passion to help others live fearlessly. Our emphasis is not on figures but on individual stories. In over 70 countries, patients, doctors and partners alike depend on Auxein Medical to move forward. Every orthopaedic implant that we manufacture is built according to the highest quality standards. We take special pride in our dedicated team of experts that makes sure we stay in line with the stringent norms set by EN ISO 13485:2012, CE and US FDA 510K – a feat few in the industry have achieved. http://www.auxein.com

Filed Under: CORPECTOMY DEVICES, NEWS

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