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Medtronic Announces FDA Approval of Minimally Invasive Device to Treat Hypertension

Approval is the culmination of 10 years of clinical research and development of the Medtronic renal denervation technology

United statesRaymond townsendJason weidmanSymplicity spyralDavid kandzariMedtronic symplicityDepartment of internal medicine renalCardiovascular serviceUniversity of pennsylvaniaPiedmont heart instituteSchool of medicineGlobal clinical programDrug administrationUnited states foodRenal denervationCardiovascular portfolio

FDA approves second renal denervation device to treat hypertension

FDA approves second renal denervation device to treat hypertension
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Byregina schafferErik swainGeorged dangasHerbertd aronowBenson fordRaymondr townsendJason weidmanMichaela wiener cardiovascular instituteIcahn school of medicine at mount sinaiSociety for cardiovascular angiographyHypertension programHospital of the university pennsylvaniaCardiology at henry ford healthSystem devices panelMedical devices advisory committeeRecor medical

Medtronic claims long-sought FDA approval in renal denervation

Medtronic claims long-sought FDA approval in renal denervation
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FDA approves Medtronic Symplicity Spyral renal denervation (RDN)

Following the FDA approval, Medtronic said it plans for immediate commercialization of its Symplicity Spyral system for hypertension.

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Medtronic announces FDA approval of minimally invasive device to treat hypertension

The Symplicity™ blood pressure procedure offers patients a new adjunct approach to lowering blood pressure Approval is the culmination of ten years of clinical research and development of the.

United statesDavid kandzariKrystin haywardSymplicity spyralMedtronic symplicityRyan weispfenningRaymond townsendJason weidmanCardiovascular serviceUniversity of pennsylvania school medicineDepartment of internal medicine renalOur missionExchange commissionPiedmont heart instituteGlobal clinical programDrug administration