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Medtronic, Inc.

FDA 510(k) & PMA Approved Devices — 141 products

Total Devices141
Categories58
Latest FDA decision2026-08-28
TypeNumberDevice NameCodeDateActions
PMA P930039 Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodesNVN2026-06-24 View
PMA P140017 Pulmonary valve prosthesis percutaneously deliveredNPV2026-06-09 View
PMA P200046 Pulmonary valve prosthesis percutaneously deliveredNPV2026-06-01 View
PMA P140010 Drug-Eluting Peripheral Transluminal Angioplasty CatheterONU2026-05-28 View
PMA P240036 Permanent defibrillator electrodesNVY2026-04-24 View
510(k) K260195 Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeDWF2026-04-23 View
PMA P950024 Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodesNVN2026-04-15 View
PMA P120017 permanent pacemaker ElectrodeDTB2026-04-15 View
PMA P980050 Implantable cardioverter defibrillator (non-CRT)LWS2026-04-15 View
PMA P990064 replacement Heart-valveDYE2026-03-03 View
510(k) K253203 Retrograde Coronary Sinus Perfusion CannulaeDWF2026-02-19 View
PMA P980043 replacement Heart-valveDYE2026-02-12 View
PMA P970031 heart-valve, non-allograft tissueLWR2026-02-12 View
PMA P060039 Drug eluting permanent left ventricular (lv) pacemaker electrodeOJX2026-02-10 View
510(k) K253998 Clearview Intracoronary ShuntsDWF2026-01-20 View
510(k) K251831 Bio-Medicus Life Support Catheter and IntroducerQHW2026-01-15 View
510(k) K253511 Concerto Versa™ Detachable CoilKRD2026-01-14 View
510(k) K253409 C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48)DQY2025-12-19 View
PMA P200028 Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillationOAE2025-10-10 View
510(k) K251258 MC2™ Two-Stage Venous Cannula; MC2X™ Three-Stage Venous CannulaDWF2025-06-20 View

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Related Clinical Trials

NCT00271180Product Performance Report: Evaluate Long-term Reliability & Performance of Medtronic Marketed Cardiac Therapy ProductsRECRUITINGNCT07005232Lead Evaluation for Defibrillation and Reliability Post Approval StudyENROLLING_BY_INVITATIONNCT07507422Post Market Evaluation of Real World Outcomes and Durability to Support Implantable Inceptiv™ Spinal Cord Stimulation TherapyRECRUITINGNCT01516723Hybrid Sirolimus-eluting Versus Everolimus-eluting Stents for Total Coronary OcclusionsCOMPLETEDNCT01586910Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Severe, Symptomatic Aortic Stenosis in Intermediate Risk Subjects Who Need Aortic Valve Replacement (SURTAVI).ACTIVE_NOT_RECRUITINGNCT01675440Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptomatic Severe Aortic Stenosis With Significant Comorbidities in Extreme Risk Subjects Who Need Aortic Valve ReplacementCOMPLETEDNCT01984710Deep Brain Stimulation for Treatment Resistant Depression With the Medtronic Activa PC+SACTIVE_NOT_RECRUITINGNCT02088554PERIGON Pivotal TrialACTIVE_NOT_RECRUITINGNCT02701283Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk PatientsACTIVE_NOT_RECRUITINGNCT03242642Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System in Patients With Severe Symptomatic Mitral Regurgitation.RECRUITING
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