Osteogenesis Stimulator - JA DME
- Standard Documentation Requirements for All Claims Submitted to DME MACs
- Clinician's Checklist [PDF]
- Documentation Checklist Osteogenesis Stimulators [PDF]
|Devices coded E0747, E0748 and E0760 are classified by the Food and Drug Administration 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.