FDAnews
www.fdanews.com/articles/100587-medtronic-gets-fda-ok-for-overactive-bladder-treatment-study

Medtronic Gets FDA OK for Overactive Bladder Treatment Study

November 2, 2007

Medtronic Inc. (MDT) said it has begun the InSite Trial, a post-market study of its commercially available InterStim treatment for overactive bladder and urinary retention, after receiving approval from the Food and Drug Administration.
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