Product analysis the device was returned with the distal flush tool (dft) positioned over the nosecone, (photo 5).The dft could not be retracted, and an inspection of the nosecone found a bulge/rupture in the centre of the nosecone, (photo 6).Medtronic is submitting this report to comply with fda reporting regulations under 21 cfr parts 4 and 803.This report is based upon information obtained by medtronic, which the company may not have been able to fully investigate or verify prior to the date the report was required by the fda.Medtronic has made reasonable efforts to obtain more complete information and has provided 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.In particular, this report does not constitute an admission by anyone that the product described in this report has any ¿defects¿ or has ¿malfunctioned¿.These words are included in the fda 3500a form and are fixed items for selection created by the fda to categorize the type of event solely for the purpose of regulatory reporting.Medtronic objects to the use of these words and others like them because of the lack of definition and the connotations implied by these terms.This statement should be included with any information or report disclosed to the public under the freedom of information act.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
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It was reported that a hawkone atherectomy device was used to treat a moderately calcified, fibrous plaque lesion with 90% stenosis in the left superficial femoral artery.Artery diameter was 5-6mm.Lesion length was 300mm.A sheath french size of 6/65 was used.A terumo, destination guidewire was used.Embolic protection was not used.The vessel was pre-dilated.The vessel was post-dilated.Ifu (instruction for use) was followed during preparation, procedure, post-procedure.It was reported that the none cone was packed too full and could not be reused.It was slightly difficult retracting none cone from sheath.No patient injury.When the device was returned to the manufacturing facility it was noted that the device was damaged.
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