B3: the actual event date is unknown.Therefore, 17-dec-2020 is used as the event date.H3: code "other" was selected as the medical device remains implanted.Return not possible.H6: a review of the manufacturing records for the device could not be performed as a valid lot number was not provided.W.L.Gore & associates, inc.(gore) is submitting this report to comply with 21 c.F.R.Part 803, the medical device reporting regulation.This report is based upon information obtained by gore, which the company may not have been able to fully investigate or verify prior to the date the report was required by the fda.Blank fields present on this report include required fields and fields determined to be not applicable.Blank required fields indicate that the information was not provided, was deemed unavailable or was not applicable.This report does not constitute an admission or a conclusion by fda, gore, or its associates that the device, gore or its associates caused or contributed to the event described in the report.In particular, this report does not constitute a legal admission by anyone that the product described in this report has any defects or has malfunctioned, as defined from a legal standpoint.These words are included in the report and are fixed items for selection created by the fda, to categorize the type of event solely for the purpose of reporting pursuant to part 803.This statement should be included with any information or report disclosed to the public under the freedom of information act.
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The following was reported to gore: on an unknown date, a stent graft which was a potential for a gore® tag® conformable thoracic stent graft with active control system was implanted (details unknown).On (b)(6) 2020, a reintervention was performed.A gore® tag® conformable thoracic stent graft with active control system was implanted distally of the previous implanted device which was potential for the gore® tag® conformable thoracic stent graft with active control system.It is unknown why this reintervention was performed.
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