Osteogenesis Stimulator

Coverage

Documentation

Probationary Prior Authorization (PPA) program

The Probationary Prior Authorization (PPA) program provides an additional layer of oversight for newly enrolled DMEPOS suppliers and suppliers that have completed a change of ownership. Under this nationwide program, selected items require prior authorization during a one-year provisional period. Beginning October 15, 2026, two osteogenesis stimulator HCPCS codes will be added.

Probationary Prior Authorization (PPA) HCPCS codes

HCPCS Effective Date Description
E0747 October 15, 2026 OSTEOGENESIS STIMULATOR, ELECTRICAL, NON-INVASIVE, OTHER THAN SPINAL APPLICATIONS
E0748 October 15, 2026 OSTEOGENESIS STIMULATOR, ELECTRICAL, NON-INVASIVE, SPINAL APPLICATIONS

Prior Authorization Timelines

Policy Initial Review Decision Timeframe Expedited Review Decision Timeframe PAR Decision Valid
Osteogenesis Stimulator 5 business days (not to exceed 7 calendar days) 2 business days 60 days

Documentation to Include in PA Package Submission

  • Osteogenesis PA request coversheet
  • Face-to-Face Evaluation (F2F)
  • Written Order Prior to Delivery (WOPD)
    • Must be completed within six (6) months after the required face-to-face encounter
  • Any additional medical records providing support for medical necessity
  • Documentation must be submitted to the appropriate jurisdiction based on the beneficiary's permanent address with the PA coversheet for fax, mail, or electronic submission of medical documentation (esMD). For Noridian Medicare Portal (NMP) submissions, complete all required fields in the portal as a coversheet is not required.

To ensure process efficiency, assure all components are completed and included within the submission.

Tips

KF Modifier

Effective for any dates of service billed, claims for devices coded E0747, E0748, and E0760 must include the KF modifier. Codes E0747, E0748, and E0760 billed without a KF modifier will be rejected as missing information.

Last Updated Sep 24 , 2026

Related Articles