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Percutaneous ultrasonic ablation of soft tissue, also known as percutaneous ultrasonic fasciotomy and percutaneous ultrasonic tenotomy, is a minimally invasive procedure used for the aspiration, fragmentation, and emulsification of soft tissue. It is associated with the surgical treatment of many conditions of the musculoskeletal system such as tendinopathy and fasciopathy.
These procedures are performed using devices known as the TX1™ Tissue Removal System and the TENEX Health TX™ System. The TX1™ and TENEX Health TX™ System use ultrasound technology to pinpoint the location of damaged tissue while using the device’s microtip to deliver ultrasonic energy, removing damaged tissue while stimulating a healing response. The TENEX Health TX™ System was cleared for marketing by the U.S. Food and Drug Administration (FDA) through the 510(k) process, recognizing this device as substantially equivalent to the predicate TX1™ Tissue Removal System device.
Percutaneous ultrasonic ablation of soft tissue is considered EXPERIMENTAL/INVESTIGATIVE for all indications, including but not limited to the following conditions, due to a lack of clinical evidence demonstrating an impact on improved health outcomes:
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Medicaid products may provide different coverage for certain services, which may be addressed in different policies. For Minnesota Health Care Program (MHCP) policies, please consult the MHCP Provider Manual website.
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Note that services with specific coverage criteria may be reviewed retrospectively to determine if criteria are being met. Retrospective denial of claims may result if criteria are not met.
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Acknowledgements:
CPT® codes copyright American Medical Association® 2023. All rights reserved.
CDT codes copyright American Dental Association® 2023. All rights reserved.