It was reported the patient¿s system was explanted due to a possible allergy.It was noted impedance testing, reprogramming, and x-rays were performed.It was reported the patient experienced increased pain.It was noted stimulation covered the pain.It was reported the patient had worsening spinal stenosis.It was noted the stimulation worked for four months, but then the patient had increasing symptoms.
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Concomitant medical products: product id 977a260, serial# (b)(4), implanted: (b)(6) 2014, explanted: (b)(6) 2014, product type: lead; product id 977a260, serial# (b)(4), implanted: (b)(6) 2014, explanted: (b)(6) 2014, product type: lead; product id neu_ptm_prog, serial# unknown, product type: programmer, patient.(b)(4).
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