Device was used for treatment, not diagnosis.Patient information is not available for reporting.Date of event: date unknown.Additional device product code are: mni, mnh, kwp, kwq.This report is for 3 unknown screws.Part and lot numbers were not provided by reporter.Udi: unknown part number, udi is unavailable.Implant date unknown.The subject device is not expected to be returned to the synthes manufacturer for evaluation.(b)(4).This report is for 3 unknown screws.Without a lot number the device history records review could not be completed.The investigation could not be completed; no conclusion could be drawn, as no product was received.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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