Ablation systems
MicroThermX Microwave Ablation System
A mains electricity (AC-powered) device intended to generate microwave energy for localized non-vascular soft-tissue ablation, typically to treat tumours, hydatid cysts and/or menorrhagia. The generator connects via a delivery cable to a probe (not included) for delivery of microwaves to the target tissues. It is intended to be used in percutaneous, laparoscopic, natural orifice or open surgery procedures to ablate tissue typically in the liver, lung, pancreas, kidney, and uterus (e.g., endometrial ablation).
MicroThermX Microwave Ablation System models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| MTX-180 | — | Not stated | Available |
| MTX-180-T2 | — | Not stated | Available |
FDA clearances
- 510(k) K141785 March 2015
Procedures that use ablation systems
Frequently asked questions
What is MicroThermX Microwave Ablation System used for?
A mains electricity (AC-powered) device intended to generate microwave energy for localized non-vascular soft-tissue ablation, typically to treat tumours, hydatid cysts and/or menorrhagia. The generator connects via a delivery cable to a probe (not included) for delivery of microwaves to the target tissues. It is intended to be used in percutaneous, laparoscopic, natural orifice or open surgery procedures to ablate tissue typically in the liver, lung, pancreas, kidney, and uterus (e.g., endometrial ablation).
Who makes MicroThermX Microwave Ablation System?
MicroThermX Microwave Ablation System is made by Perseon Corporation. It is listed under tumor ablation systems (microwave, rf, cryo) in our device library.
What sizes does MicroThermX Microwave Ablation System come in?
The FDA device database does not list sizes for MicroThermX Microwave Ablation System. Check the instructions for use or ask a Perseon Corporation representative.
Is MicroThermX Microwave Ablation System MRI safe?
The FDA device database entry for MicroThermX Microwave Ablation System does not state its MRI safety status. Check the labeling before MRI.
Is MicroThermX Microwave Ablation System FDA cleared?
MicroThermX Microwave Ablation System is covered by FDA submission K141785.
How do I contact a Perseon Corporation sales representative?
Perseon Corporation has not listed representatives on LA Vascular yet. Visit the Perseon Corporation company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.