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karl storz scb covidien forcetriad interface module
Karl Storz Endoscopy-America
Summary: The Karl Storz SCB Covidien ForceTriad Interface Module is a medical device used for tumor ablation procedures. It is primarily utilized by surgeons and interventional radiologists in oncology settings.
FDA Clearance Information
Pathway
510K
Number
K111165 ↗
Decision Date
January 6, 2012
Product Code
ODA
Device Class
Class 2
Evidence
0 studies
The device was cleared through the FDA 510(k) pathway on January 6, 2012. It is manufactured by Karl Storz Endoscopy-America and classified as a Class 2 device under product code ODA.
What It Is
The Karl Storz SCB Covidien ForceTriad Interface Module is designed to integrate with the Covidien ForceTriad energy platform, facilitating advanced energy delivery for surgical procedures. It enables precise control of energy output, which is crucial for effective tumor ablation. The device enhances the functionality of existing surgical systems by providing seamless interface capabilities.
Clinical Applications
This device is commonly used in surgical oncology for the ablation of tumors. It is particularly useful in settings where precise energy delivery is required, such as in liver, kidney, or lung tumor ablations. Surgeons and interventional radiologists in hospital operating rooms or specialized cancer treatment centers are the primary users.
Indications for Use
The device is indicated for use in procedures requiring tumor ablation, which involves destroying cancerous tissue using focused energy. It is suitable for patients with tumors that are accessible via surgical or minimally invasive techniques.
Practical Considerations
The interface module is compatible with the Covidien ForceTriad energy platform, ensuring easy integration into existing surgical setups. Clinicians should be familiar with the energy settings and compatibility requirements to optimize performance during procedures.
Frequently Asked Questions
What is the Karl Storz SCB Covidien ForceTriad Interface Module used for?
It is used for tumor ablation procedures, allowing precise energy delivery to destroy cancerous tissues.
What specialties typically use this device?
Surgeons and interventional radiologists, particularly those specializing in oncology, commonly use this device.
What are the FDA-cleared indications?
The device is indicated for tumor ablation in patients with accessible tumors, using surgical or minimally invasive techniques.
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.