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resprocessed serfas energy probe
Stryker Sustainability Solutions
Summary: The Resprocessed Serfas Energy Probe is a medical device used for tumor ablation. It is primarily used by surgeons and interventional radiologists in oncology settings.
FDA Clearance Information
Pathway
510K
Number
K121855 ↗
Decision Date
August 16, 2012
Product Code
NUJ
Device Class
Class 2
Evidence
0 studies
The Resprocessed Serfas Energy Probe was cleared via the FDA 510k pathway on August 16, 2012. It is manufactured by Stryker Sustainability Solutions and classified as a Class 2 device.
What It Is
The Resprocessed Serfas Energy Probe is a surgical instrument designed for the ablation of tumors. It uses energy to destroy cancerous tissue, providing a minimally invasive option for tumor management. The device is reprocessed, indicating it is designed for multiple uses after proper sterilization, aligning with sustainability practices in healthcare.
Clinical Applications
This device is commonly used in oncology for the ablation of solid tumors. It is utilized in both surgical and interventional radiology settings, often in hospitals or specialized cancer treatment centers. The probe is suitable for patients with tumors that are difficult to access or inoperable by traditional surgical means.
Indications for Use
The FDA indications suggest that the Resprocessed Serfas Energy Probe is intended for patients requiring tumor ablation. It is particularly useful for those with localized tumors that can be targeted with energy-based techniques.
Practical Considerations
The device is typically available in various sizes to accommodate different tumor sizes and locations. It is compatible with standard surgical and radiological equipment, and clinicians should be trained in its specific energy delivery technique to ensure optimal outcomes.
Frequently Asked Questions
What is Resprocessed Serfas Energy Probe used for?
It is used for the ablation of tumors, particularly in cases where minimally invasive techniques are preferred.
What specialties typically use this device?
Oncology surgeons and interventional radiologists are the primary users of this device.
What are the FDA-cleared indications?
The device is indicated for the ablation of tumors, providing a treatment option for patients with localized cancerous growths.
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.