Spinal bone growth stimulators
Non-invasive osteogenesis stimulators worn after spinal fusion surgery to support bone healing. We carry devices from the major manufacturers and handle the documentation that goes with them.
A worn device, not an implant
A spinal bone growth stimulator (also called an osteogenesis or "bone" stimulator) is a non-invasive device the patient wears against the back for a prescribed period each day. It is intended to support bone healing along a spinal fusion. Nothing is implanted and use is not painful — the patient simply wears it on a schedule for the treatment episode.
Coverage of E0748 is decided on clinical review under Local Coverage Determination L33796 (Osteogenesis Stimulators) by the DME MAC — Noridian in Jurisdiction D (Washington and Oregon). There is no prior-authorization requirement and no Written Order Prior to Delivery requirement for E0748; the standard SWO and face-to-face documentation apply.
Quick facts
- HCPCSE0748
- Governing LCDL33796 — Osteogenesis Stimulators
- Prior authorizationNot required
- Default dispensingNU (new purchase) · 270-day single treatment episode
- DocumentationStandard Written Order (A55426) + face-to-face within 6 months (42 CFR 410.38)
Manufacturers & models
We stock spinal stimulators from the manufacturers clinicians most often request:
Zimmer Biomet
SpinalPak II — non-invasive spinal fusion stimulator.
Enovis / DJO
SpinalLogic — compact non-invasive spinal bone growth stimulator.
Orthofix
Spinal-Stim for lumbar fusion. Cervical-Stim available on request for cervical fusion.
Have a preferred device or a payer that prefers a particular model? Tell us when you send the order and we'll match it.
How to order E0748
E0748 Standard Written Order
Fillable PDF · 45 KB · covers Biomet SpinalPak, Enovis SpinalLogic, Orthofix Spinal-Stim and Cervical-Stim · captures the six required SWO elements per CMS Article A55426 · every field on this form is fillable in any PDF reader.
Complete the SWO
Open the order form above in a PDF reader (Adobe, Preview, browser), fill in the patient and prescriber sections, and have the treating practitioner sign. Documentation requirement: the face-to-face encounter must be within the prior six months.
Send it to us
Fax to 509-980-7062 or email the completed form to rx@petersonmedicalequipment.com from a secure channel. Questions? Call 509-783-7501.
We dispense & instruct
We deliver the device, walk the patient through wear schedule and use, and archive the order and supporting documentation.
Documentation questions? Ask the coverage assistant — for example, "what does a Standard Written Order for E0748 need to include?" — or call us. It is general reference only, not a coverage guarantee, and not for patient details.
Send an E0748 order
Fax a completed SWO to 509-980-7062 or call us — we'll handle the rest.