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The ANS Neurostimulation system is indicated for Spinal Cord Stimulation (SCS) in the treatment of chronic pain of trunk and limbs, either as the sole mitigating agent, or as an adjunct to other modes of therapy used in a multidisciplinary approach.

The Rapid Programmer is intended to assist clinicians in determining the optimum performance while automatically logging procedures data. Rapid Programmer also allows the clinician to optimize performance by leading the patient through a series of device parameter combinations and recording the stimulation effects. This system uses a touch screen computer to program the stimulator to the required waveforms and electrode configurations and to log the information derived.

This system uses a touch screen computer to program the stimulator to the required waveforms and electrode configurations and to log the information derived.

I am sorry, but the provided text does not contain information about the acceptance criteria or the study that proves the device meets the acceptance criteria. The document is a 510(k) premarket notification letter from the FDA regarding the Rapid Programmer device, Models 3830 and 3831. It primarily discusses the substantial equivalence determination and the regulatory requirements for the device.

Therefore, I cannot extract the requested information to fill in the table or answer the specific questions about device performance studies.

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