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Commercial product medical coverage policy for interspinous and interlaminar stabilization/distraction devices (spacers) for treatment of lumbar spinal stenosis and related indications; defines medical necessity determinations, exclusions, coding, and references. Not applicable to Medicare Advantage (see related policies).
No material clinical/coverage changes
Policy scope: Commercial products only; not applicable to Medicare Advantage (see related policies). Effective date: 02/01/2023; Last review: 05/07/2025. Headline stance: Interspinous and interlaminar spacers are not medically necessary when used as stand-alone spacers for lumbar spinal stenosis and neurogenic claudication, and interlaminar stabilization following decompression surgery is also considered not medically necessary. Removal of devices for medical reasons (device failure, infection, etc.) requires individual review for medical necessity and there is no specific CPT code for removal (report appropriate unlisted CPT).
Covered / Not Medically Necessary Determinations
Policy statements for Commercial Products:
| 22867 | Insertion of interlaminar/interspinous process stabilization/distraction device, without fusion, including image guidance when performed, with open decompression, lumbar; single level. |
| 22868 | Insertion of interlaminar/interspinous process stabilization/distraction device, without fusion, including image guidance when performed, with open decompression, lumbar; second level (list separately in addition to code for primary procedure). |
| 22869 | Insertion of interlaminar/interspinous process stabilization/distraction device, without open decompression or fusion, including image guidance when performed, lumbar; single level. |
| 22870 | Insertion of interlaminar/interspinous process stabilization/distraction device, without open decompression or fusion, including image guidance when performed, lumbar; second level (list separately in addition to code for primary procedure). |
| C1821 | Interspinous distraction device (implantable) process |
| UNLISTED | No specific CPT code for removal of interlaminar/interspinous process stabilization/distraction devices; appropriate unlisted CPT code should be used. |
Review device removal for medical necessity
Removal for medical reasons (device failure, infection, etc.) must be reviewed for medical necessity per related policy 'Removal of Implantable Devices'.
Use unlisted CPT for device removal
Because there is no specific CPT code for removal of interlaminar/interspinous spacers, report an appropriate unlisted CPT code for removal procedures.
Interspinous and interlaminar spacers are implants placed between spinous processes or between adjacent lamina and spinous processes to distract the neural foramina, restrict extension, and provide dynamic stabilization for patients with lumbar spinal stenosis and neurogenic claudication. The evidence base includes randomized controlled trials, systematic reviews, and observational/claims studies. Overall study results are mixed: some trials (for example the Superion pivotal trial) reported improvements in some quality-of-life domains, but other trials (for example the coflex/FELIX trials) demonstrated substantially higher reoperation rates with implants compared with decompression. Systematic reviews and comparative analyses have shown increased reoperation rates and no consistent, significant improvements in pain, function, or quality-of-life outcomes. Consequently, the evidence is considered insufficient to demonstrate a net health benefit for routine use of these devices.
Key Evidence
Definitions
See related policy 'Removal of Implantable Devices' for review details.
Exceptions / FDA Indications (evidence summary, not coverage)
Devices and FDA-labeled indications discussed in evidence section (policy does not equate to coverage):