510k: this report is for an unknown rafn nail/unknown lot.Part and lot number are unknown; udi number is unknown.Complainant part is not expected to be returned for manufacturer review/investigation.Without a lot number the device history records review could not be completed.Product was not returned.Based on the information available, it has been determined that no corrective and/or preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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It was reported that the patient underwent a procedure on an unknown date, with retrograde approach for a poly trauma at femoral shaft.Postoperatively, there was no union of fracture noted and patient had an open femur with ipsilateral multiligamentous knee instability and heel degloving.Patient experienced pain and was scheduled for non-union surgery 11 months ago but never showed up for surgery and has never been seen.There was an evidence of healing reported.No further information is available.This report is for an unknown rafn nail.This is report 1 of 1 for (b)(4).
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