Product Classification

• Device: drug eluting permanent left ventricular (lv) pacemaker electrode
• Definition: Drug eluting permanent lv pacemaker electrodes are used with compatible cardiac rhythm therapy (crt) devices to deliver pacing pulses to the heart.
• Physical State: The device is a flexible, insulated electrical conductor with one end designed to make a secure connection to a CRT device and the other end located in a left cardiac vein.
• Technical Method: Used as part of an implantable crt system.
• Target Area: Makes contact with the lv via the left cardiac vein.
• Review Panel: Cardiovascular
• Product Code: OJX
• Premarket Review: Cardiac Electrophysiology, Diagnostics, and Monitoring Devices (DHT2A); Cardiac Electrophysiology, Diagnostics, and Monitoring Devices (DHT2A)
• Submission Type: PMA
• Device Class: 3
• Total Product Life Cycle (TPLC): TPLC Product Code Report
• GMP Exempt?: No
• Summary Malfunction Reporting: Ineligible
• Implanted Device?: Yes
• Life-Sustain/Support Device?: Yes

Recognized Consensus Standards

• 3-89 ISO 27186 First edition 2010-03-15
  Active implantable medical devices - Four-pole connector system for implantable cardiac rhythm management devices - Dimensional and test requirements
• 3-132 ISO 27185 First edition 2012-02-15
  Cardiac Rhythm Management Devices - Symbols to be Used With Cardiac Rhythm Management Device Labels, and Information to be Supplied - General Requirements
• 3-143 ISO 12417-1 First edition 2015-10-01
  Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements
• 3-185 AAMI ANSI PC76:2021
  Active implantable medical devices - Requirements and test protocols for safety of patients with pacemakers and ICDs exposed to magnetic resonance imaging
• 3-193 ISO 12417-1 Second edition 2024-02
  Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements

Third Party Review

Not Third Party Eligible