Synthes is submitting this report as a result of remediation activities.Device listed in this report is used for treatment, not diagnosis.Any additional information received regarding this event after filing this report shall be filed on a supplemental mdr.Device history record review was conducted.The dhr review shows this device being manufactured, etched, inspected, ultrasonically cleaned and delivered to the brw plant on (b)(6) 2012.There were no nonconformance¿s noted for this device.Placeholder.
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