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cordis ducor ptr system
Cordis
Summary: The Cordis Ducor PTR System is a medical device used primarily in vascular procedures to assist with venous stenting. It is typically utilized by interventional radiologists and vascular surgeons.
FDA Clearance Information
Pathway
510K
Number
K811971 ↗
Decision Date
August 13, 1981
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
The Cordis Ducor PTR System was cleared through the FDA 510(k) pathway on August 13, 1981. It is manufactured by Cordis and classified as a Class 2 device under product code DQY.
What It Is
The Cordis Ducor PTR System is a percutaneous transluminal recanalization system designed to facilitate the placement of venous stents. It operates by providing a pathway for stent delivery in obstructed or narrowed veins, aiding in the restoration of normal blood flow. This device is particularly useful in treating conditions that involve venous insufficiency or obstruction.
Clinical Applications
This device is commonly used in procedures involving the treatment of venous obstructions, such as those found in patients with chronic venous insufficiency or post-thrombotic syndrome. It is typically employed in hospital settings by interventional radiologists and vascular surgeons. The patient population often includes those with a history of deep vein thrombosis or other venous disorders.
Indications for Use
The Cordis Ducor PTR System is indicated for use in patients requiring venous stenting due to conditions like venous obstruction or insufficiency. It is particularly beneficial for patients experiencing symptoms related to impaired venous blood flow.
Practical Considerations
When using the Cordis Ducor PTR System, clinicians should consider the appropriate sizing of the stent for the specific vein being treated. Compatibility with existing stenting systems and familiarity with percutaneous techniques are essential for optimal outcomes.
Frequently Asked Questions
What is the Cordis Ducor PTR System used for?
It is used for facilitating the placement of venous stents in patients with venous obstructions or insufficiencies.
What specialties typically use this device?
Interventional radiologists and vascular surgeons commonly use this device.
What are the FDA-cleared indications?
The device is indicated for use in patients needing venous stenting due to venous obstruction or insufficiency.
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.