Device was used for treatment, not diagnosis.Patient initials (b)(6).Patient weight not provided by reporter.Unknown when non-union, pain, discomfort or irritation occurred.Additional product codes: mni, mnh, kwp, kwq.(b)(4) lot number unknown device is not expected to be returned for manufacturer review/investigation.Subject device has not been received.Without a lot number, the device history record review and 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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