Heather S. Rosecrans serves as Vice President of Regulatory Affairs at the Medical Device Manufacturers Association. Previously, Heather was the Director of the Premarket Notification (510(k)) Staff, Program Operations Staff, Office of Device Evaluation, Center for Devices and Radiological Health (CDRH), U.S. Food and Drug Administration. While at the FDA, Heather was responsible for administrating the 510(k), classification, reclassification, 513(g), and class II petitions for exemption programs for CDRH.