Expert in function and utilization of cardiovascular and/or interventional medical devices (e.g., angioplasty balloons, vascular stents, carotid stent systems, EVAR grafts, TEVAR devices, mechanical thrombectomy systems, AV grafts, dialysis catheters, venous stents, endovenous ablation systems, introducer sheaths, intravascular ultrasound, etc.) to include specific knowledge of non-invasive devices and instruments used for diagnosis; invasive devices, such as implantable devices; and surgical systems. In general, these consultants provide consultation related to supporting medical device reviews (EUA, 510(k), PMA, HDE and De Novo marketing applications, Pre-submissions, Investigational Device Exemptions, Recalls); participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders; develop written reviews and correspondence; perform research; conduct data analysis; write detailed documents and reports; and execute other administrative office tasks related to CDRH's projects.