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FDA PMA

Drug eluting permanent left ventricular (lv) pacemaker electrode

PMA Number: P060039 · 2026-02-10

ApplicantMedtronic, Inc.
Decision Date2026-02-10
PMA NumberP060039
Product CodeOJX
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

Drug eluting permanent left ventricular (lv) pacemaker electrode is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2026-02-10. The device is classified under product code OJX. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Drug eluting permanent left ventricular (lv) pacemaker electrode?

Drug eluting permanent left ventricular (lv) pacemaker electrode is a medical device that received FDA 510(k) clearance on 2026-02-10. The listed applicant is Medtronic, Inc..

When did Drug eluting permanent left ventricular (lv) pacemaker electrode receive FDA 510(k) clearance?

The clearance date for Drug eluting permanent left ventricular (lv) pacemaker electrode can be found in the official FDA records.

Who is the listed applicant for Drug eluting permanent left ventricular (lv) pacemaker electrode?

The FDA 510(k) record lists Medtronic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Drug eluting permanent left ventricular (lv) pacemaker electrode?

The FDA product code for Drug eluting permanent left ventricular (lv) pacemaker electrode is OJX.

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.

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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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