Medtronic announced that the first patient has been enrolled in the ENDURANCE Post-Approval Study (PAS) evaluating the Altaviva™ implantable tibial neuromodulation (ITNM) device for the treatment of urge urinary incontinence. The first study procedure was successfully performed by Vincent R. Lucente, MD, MBA, FACOG, FPMRS at Axia Women's Health in Allentown, Pennsylvania.
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