Model Number MSB_UNK_SCREW |
Device Problem
Device Dislodged or Dislocated (2923)
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Patient Problem
Intervertebral Disc Compression or Protrusion (4524)
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Event Date 12/21/2022 |
Event Type
malfunction
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Manufacturer Narrative
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D4, g4: product identifiers are unknown.H6 - neither the device nor films of applicable imaging studies were returned to the manufacturer for evaluation.Therefore, we are unable to determine the definitive cause of the reported event.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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Event Description
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Information was received from multiple sources (manufacturer representative, healthcare provider, clinical study) regarding an event which occurred post a clinical study (study id: (b)(4)) transforaminal lumbar interbody fusion procedure in a patient (clinical id: (b)(4)).Patient medical history: raynauds, hypertension, mild blockage of coronary arteries, sjogrens syndrome, bilateral lower extremity pain, low back pain, peridontal disease, gum disease, anxiety and depression, substance use: tobacco it was reported that there was a mildly increased l3-4 anterolisthesis measuring 3cm.Lucency surrounding the l3 and l5 screws bilaterally was suggestive of loosening per 12 month lumbar ct scan report. no malfunction was reported for the cage.There were no further complications reported regarding the event.
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Search Alerts/Recalls
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