Threat modeling and performing a risk assessment are required by the FDA as part of a 510(k) pre-market submission and will tell you what cybersecurity is needed to make sure your medical device is secure. Webinar presenters will go step-by-step through a threat model and risk assessment for a number of attack paths to clearly show how it is done. By the end of the webinar you will have a very good idea of how to develop a cybersecurity threat model and to perform risk analysis.