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www.fdanews.com/articles/171164-stimguard-receives-fda-ide-designation-for-microsize-bladder-device

StimGuard Receives FDA IDE Designation for Microsize Bladder Device

May 11, 2015

StimGuard’s wireless microsize Overactive Bladder Syndrome implantable device, capable of being placed completely through a needle, has won an Investigational Device Exemption from the FDA, the devicemaker announced Monday.

Unlike traditional OAB treatment, which requires a large implantable pulse generator, the device does not require a surgical incision. Rather, the product uses the Stimwave electroceutical microchip to administer small energy pulses to electrodes near surrounding nerves.

The device’s treatment therapy, Sacral Nerve Stimulation, has been FDA-approved for severe OAB since 1997.

A clinical trial is scheduled for this summer. More than 33 million people are afflicted with OAB in the U.S. — Jason Scott