White Paper
Adverse Event Reporting – An FDA Requirement: What, When, Who & How
Presented in 2010
Most orthopaedic surgeons in the course of their practice will encounter and explant medical devices which have failed. Such failures may simply resuMost orthopaedic surgeons in the course of their practice will encounter and explant medical devices which have failed. Such failures may simply result from long-term in-vivo device usage, component material breakdown, technique at…

