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cordis ancor active fixation lead
Cordis
Summary: The Cordis Ancor Active Fixation Lead is a medical device used in cardiac procedures to secure leads within the heart. It is primarily used by cardiologists and electrophysiologists.
FDA Clearance Information
Pathway
510K
Number
K832422 ↗
Decision Date
August 5, 1986
Product Code
DTB
Device Class
Class 3
Evidence
0 studies
The Cordis Ancor Active Fixation Lead was cleared through the FDA 510k pathway on August 5, 1986. It is manufactured by Cordis and classified as a Class III device.
What It Is
The Cordis Ancor Active Fixation Lead is a specialized lead used in cardiac pacing and defibrillation procedures. It features an active fixation mechanism that allows it to be securely attached to the heart tissue, ensuring stable electrical conduction. This device is crucial for maintaining proper heart rhythm in patients requiring pacemakers or implantable cardioverter-defibrillators (ICDs).
Clinical Applications
This device is commonly used in cardiac electrophysiology procedures, particularly in the implantation of pacemakers and ICDs. It is utilized in hospital settings by cardiologists and electrophysiologists to treat patients with arrhythmias or heart failure. The lead is suitable for a wide range of patients, including those with complex cardiac conditions requiring precise lead placement.
Indications for Use
The Cordis Ancor Active Fixation Lead is indicated for use in patients who require cardiac pacing or defibrillation. It is particularly beneficial for individuals with arrhythmias or heart block, where stable lead placement is essential for effective treatment.
Practical Considerations
The lead is available in various lengths to accommodate different patient anatomies and is compatible with most pacemaker and ICD systems. Proper technique during implantation is crucial to ensure optimal lead positioning and function.
Frequently Asked Questions
What is the Cordis Ancor Active Fixation Lead used for?
It is used in cardiac procedures to secure pacing or defibrillation leads within the heart.
What specialties typically use this device?
Cardiologists and electrophysiologists typically use this device in hospital settings.
What are the FDA-cleared indications?
The device is indicated for patients needing cardiac pacing or defibrillation, particularly those with arrhythmias or heart block.
Disclaimer: This page compiles publicly available regulatory and published clinical evidence for educational reference.
It does not constitute medical advice, product endorsement, or a recommendation for clinical use.
Always consult manufacturer documentation and clinical judgment for patient care decisions.