FDAnews Device Daily Bulletin
Medical Devices / Submissions and Approvals

SpineEX Interbody Fusion Device Gets 510(k) Clearance

Oct. 11, 2018
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The FDA cleared SpineEX’s Sagittae lateral lumbar interbody fusion (LLIF) device for use in spinal fusion surgeries.

The minimally invasive fusion procedure causes less disruption to lower back muscles because it approaches from the patient’s side, resulting in faster recovery and less blood loss.

The personalized device is expandable and offers a large graft space ideal for lumbar fusion procedures.

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