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serfas 90-s electrosurgical probe
Stryker
Summary: The Serfas 90-S Electrosurgical Probe by Stryker is a device used for tumor ablation. It is typically utilized by surgeons in oncology to remove or destroy cancerous tissues.
FDA Clearance Information
Pathway
510K
Number
K160050 ↗
Decision Date
May 3, 2016
Product Code
GEI
Device Class
Class 2
Evidence
0 studies
The Serfas 90-S Electrosurgical Probe was cleared via the FDA 510k pathway on May 3, 2016. Manufactured by Stryker, it is classified as a Class 2 medical device under product code GEI.
What It Is
The Serfas 90-S Electrosurgical Probe is an advanced surgical tool designed for the ablation of tumors. It uses electrical energy to generate heat, which is then applied to targeted tissues to destroy abnormal cells. This device is part of a broader category of electrosurgical instruments that offer precision and control during surgical procedures.
Clinical Applications
This device is commonly used in surgical oncology settings for the treatment of solid tumors. It is particularly useful in minimally invasive procedures, where precise ablation of cancerous tissue is required. Surgeons in specialties such as general surgery, gynecologic oncology, and urology may employ this probe in both inpatient and outpatient settings.
Indications for Use
The FDA-cleared indications for the Serfas 90-S Electrosurgical Probe involve the ablation of tumors. It is intended for patients with solid tumors requiring surgical intervention to remove or reduce cancerous tissue.
Practical Considerations
The Serfas 90-S Electrosurgical Probe is typically compatible with standard electrosurgical generators. Clinicians should consider the size and location of the tumor when selecting the probe size and technique. Proper training in electrosurgical techniques is essential to maximize the device's efficacy and safety.
Frequently Asked Questions
What is the Serfas 90-S Electrosurgical Probe used for?
It is used for the ablation of tumors, particularly in surgical oncology to remove or destroy cancerous tissues.
What specialties typically use this device?
Specialties such as surgical oncology, general surgery, gynecologic oncology, and urology commonly use this device.
What are the FDA-cleared indications?
The device is indicated for the ablation of tumors, specifically targeting solid tumors requiring surgical intervention.
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.