It was reported that the patient had a ¿bunch¿ of complications after the implant surgery (stated to be 3 weeks prior, and implant was 3 weeks prior).The patient had an infection and inflammation where the stimulator was placed.Both had cleared up by the report.Additional information regarding the infection including treatment was requested.If received, a follow up report will be sent.
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Concomitant medical products: product id: 97740, serial# (b)(4), product type: programmer, patient.Product id: 97754, serial# (b)(4), product type: recharger.Product id: 977a160, serial# (b)(4), implanted: (b)(6) 2014, product type: lead.Product id: 977a160, serial# (b)(4), implanted: (b)(6) 2014, product type: lead.(b)(4).
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