Information was received from a distributor, healthcare professional via a manufacturer representative regarding a patient with spinal therapy.Removal was scheduled it was reported that the one screw had been placed deviated into the spinal canal, so it was removed.It was removed and a laminectomy was performed on april 3, and the operation was completed.
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G4: this part is not approved for use in the united states; however, a similar device catalog #853-465, 510k #k050082 and udi #(b)(4) is marketed in the united states.D6a.Implant date is unknown.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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