FDA:Fda -Death Reported In Mdr Described Malfunctioning Cerelink Icp Monitor During Use In Critically Injured Patient & Was Mitigated By Replacing Icp Sensor.Fda - Cause Of Patient Death Was Determined By Integra To Be Unrelated To The Cerelink Icp Monitor Malfunction.Further Company Coverage: Iart.O. ((Reuters.Briefs@Thomsonreuters.Com;)).