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FDA PMA

Implantable cardioverter defibrillator (non-CRT)

PMA Number: P900061 · 2026-04-15

ApplicantMedtronic Cardiac Rhythm Disease Management
Decision Date2026-04-15
PMA NumberP900061
Product CodeLWS
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

Implantable cardioverter defibrillator (non-CRT) is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Cardiac Rhythm Disease Management. It received FDA 510(k) clearance on 2026-04-15. The device is classified under product code LWS. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Implantable cardioverter defibrillator (non-CRT)?

Implantable cardioverter defibrillator (non-CRT) is a medical device that received FDA 510(k) clearance on 2026-04-15. The listed applicant is Medtronic Cardiac Rhythm Disease Management.

When did Implantable cardioverter defibrillator (non-CRT) receive FDA 510(k) clearance?

The clearance date for Implantable cardioverter defibrillator (non-CRT) can be found in the official FDA records.

Who is the listed applicant for Implantable cardioverter defibrillator (non-CRT)?

The FDA 510(k) record lists Medtronic Cardiac Rhythm Disease Management as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Implantable cardioverter defibrillator (non-CRT)?

The FDA product code for Implantable cardioverter defibrillator (non-CRT) is LWS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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