Use of the KF Modifier with Osteogenesis Stimulators

The KF modifier is required if the FDA has designated that item as a Class III device. Osteogenesis stimulator devices coded E0747, E0748, and E0760 are classified by the FDA as Class III devices; therefore, all claims for codes E0747, E0748, and E0760 must include the KF modifier. Claim lines billed without a KF modifier will be rejected as missing information. Additional information can be found on the Osteogenesis Stimulators webpage.

Last Updated Sep 20 , 2023