Integra LifeSciences Receives FDA Clearance for Expanded Indication for Spinal Device


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Integra LifeSciencesHoldings Corporation (Nasdaq: IART) today announced that the Food and DrugAdministration (FDA) has approved an expanded indication for use of theIntegra® Vu aPOD™ Prime Intervertebral Body Fusion Device (IBD) in anteriorlumbar interbody fusion (ALIF) procedures. The new stand-alone indicationincludes four points of fixation, which is composed of two screws and aSpinPlate™. The Integra® Vu aPOD™ Prime IBD will be featured at the Congressof Neurological Surgeons (CNS) annual meeting, October 6 – 10, 2012, inChicago, Illinois.

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