Clariance has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its Stand-Alone Anterior Lumbar Interbody Fusion Device: Idys®-ALIF ZP 3DTi.
The design allows four fixation screws to be inserted through the cage and into the adjacent vertebral bodies to create a zero-profile stand-alone construct that removes the need for posterior fixation. Idys®-ALIF ZP 3DTi will be delivered in sterile packaging and available in multiple footprint, heights and lordotic angles.
Benefits:
- Zero profile: Zero anterior profile to avoid interference with vascular structures.
- Strong fixation:4-screw configuration with strategic angulation provides an optimal cortico-cancellous bone purchase.
- Streamlined surgical technique:With a one-step locking mechanism, self-tapping and self-drilling screws, intraoperative efficiency is increased.
About Clariance:
Clariance is a French company specialized in spine surgery. Since 2007, we have been developing solutions with excellence that improve clinical outcomes.Website http://clariance-spine.com
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