Grosse Pointe Shores, Michigan
Robert E. Lee, MD is a medical officer from the Vascular and Endovascular Devices Team in the Office of Cardiovascular Devices, Center for Devices & Radiologic Health, US Food and Drug Administration, in Silver Spring, Maryland. The Vascular and Endovascular Devices Team has the responsibility for the premarket reviews and post-market surveillance of aortic endografts, prosthetic vascular grafts, other devices used in open vascular surgery including topical hemostatic agents, venous valve substitutes, and many of the products used to create vascular access for hemodialysis or to treat dysfunctional AV access.
Dr. Lee is a native of Detroit and a graduate of the University of Michigan Medical School. He completed a general surgery residency and a vascular surgery fellowship at Henry Ford Hospital in Detroit. Dr. Lee is certified by the American Board of Surgery in both general surgery and vascular surgery. Prior to joining the FDA in January 2015, he practiced vascular and endovascular surgery in southeast Michigan for three decades. Dr. Lee is the first ABS certified vascular surgeon to serve as an FDA medical officer at the Center for Devices and Radiologic Health.
C03: Endovascular Aortic Devices: From Regulatory Approval to Post-Market Oversight
Wednesday, June 19, 2024
12:30 PM – 1:30 PM CT
Medical Device Event Reporting: Your Role in Assuring Safety of Marketed Devices
Wednesday, June 19, 2024
1:02 PM – 1:10 PM CT