Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.
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It was reported that during the implant procedure of the pacing lead sensing, impedance and threshold were noted to be inconsistent.The lead was fractured at the site of torque on the catheter and the catheter was kinked/bent.The lead and the catheter was attempted, not used and was replaced.No patient complications have been reported as a result of this event.
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