≥50% objective pain reduction (trial phase)
Missing this triggers an immediate lack-of-medical-necessity denial.
Denial-data diagnostics · CPT 63650 / 63685
Aevitex reviews your historical, de-identified denial data and shows exactly where spinal cord stimulator authorizations stall — before the next packet ships.
No live PHI · No EHR integration · Diagnostic only
Most CPT 63685 first-pass denials trace back to four payer-mandatory requirements. When one is missing or unlinked, the packet stalls.
Missing this triggers an immediate lack-of-medical-necessity denial.
Required before a permanent implant.
Required for stepwise-treatment verification.
Required to document the underlying pathology.
De-identified denial notes, EOBs, exports, spreadsheets, PDFs. No live PHI, no EHR access, no portal credentials.
An air-gapped, deterministic engine audits every 63650/63685 case against the four requirements. Nothing leaves your environment; gaps are reported, never inferred.
In seven days: a Clinical Documentation Matrix, failure modes ranked by recoverable exposure, and the workflow fixes to make before your next packet.
Every case scored against the four requirements — Yes, No, or Missing. Nothing inferred, nothing fabricated.
Sample diagnostic output (anonymized)
Synthetic sample. No PHI. Illustrative only.
If your data shows no measurable CPT 63685 denial pattern, we tell you and stop before billing the full diagnostic.
Built for independent interventional pain practices that want a credible 63685 denial diagnostic before investing in heavier automation.