Consultant, King & Spalding
Lynette Zentgraft joined King & Spalding’s FDA & Life Sciences Practice Group as a Regulatory Submissions and Strategy Expert.
Prior to joining King & Spalding, Ms. Zentgraft was a Senior Scientific Reviewer for medical devices at the Food and Drug Administration, Center for Devices and Radiological Health, Office of Device Evaluation. There, her responsibilities included the review of premarket notification (510(k)), investigational device exemption (IDE), premarket approval (PMA) and other regulatory submissions.
Ms. Zentgraft is a graduate of Rensselaer Polytechnic Institute where she received her Bachelor of Science degree in Biomedical Engineering in 1992. She also received her Masters degree in Applied Physics and Engineering in Biomedicine from Johns Hopkins University in 1998.