Return to Search
Coverage and Billing for Ultrasound Stimulation for Nonunion Fracture Healing
The "KF" modifier must be used when billing for the
Ultrasonic Osteogenic Stimulation device because it is a FDA Class III device.
Issued by: Centers for Medicare & Medicaid Services (CMS)
Issue Date: January 20, 2006
DISCLAIMER: The contents of this database lack the force and effect of law, except as authorized by law (including Medicare Advantage Rate Announcements and Advance Notices) or as specifically incorporated into a contract. The Department may not cite, use, or rely on any guidance that is not posted on the guidance repository, except to establish historical facts.