Integra LifeSciences has received FDA approval for expanded indication for use of the Integra Vu aPOD Prime Intervertebral Body Fusion Device in anterior lumbar interbody fusion procedures.
The new stand-alone indication includes four points of fixation, which is composed of two screws and a SpinPlate. The Integra Vu aPOD Prime IBD features two zero-profile options utilizing two screws or two screws and a SpinPlate to help secure the IBD in its functional position, eliminating the need for supplemental fixation implants and reducing
the number of steps and implants required to perform an ALIF procedure.
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