1. 1. Manage and understand the commercialization process for investigational devices to treat urologic diseases through a traditional FDA 510k pathway, and a de novo 510k pathway
  2. 2. Understand new/evolving techniques, technologies, and management strategies in clinical urologic care
  3. 3. Take important considerations into account for urologists outside of core practice
Session date: 
10/22/2025 - 7:00am to 8:00am CDT
Add to calendar: 
  • 1.00 AMA PRA Category 1 Credit™
  • 1.00 Participation
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Speaker Name: 
Matthew Sorensen, MD, MS, FACS