Device 2 of 2.Reference mfr.Report: 1627487-2017-08489.It was reported the patient experienced pain outside of the targeted pain area during the trial implant procedure, and shortly after the patient reported symptoms of weakness and diminished motor function.The patient also experienced ineffective stimulation despite stimulation being delivered in the targeted area.As such, the trial leads were explanted a day post-implant.However, the symptoms persisted and the patient was in a wheelchair and was unable to stand without assistance.
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