Ep eval subq impl dfb
CPT code 93644 covers the evaluation and testing of a subcutaneous implantable cardioverter-defibrillator (S-ICD), a device placed under the skin to monitor and correct dangerous heart rhythms without leads going into the heart.
This calculator gives a typical-case estimate using standard Medicare modifier rules. Actual payment depends on payer policies, documentation, code-specific CMS status indicators, and locality. Verify before billing.
RVU breakdown
Conversion factor: 32.3465 · Source: CMS MPFS RVU25A · Confidence: High
NCCI bundling edits
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Billing tips
Verify S-ICD system type before billing; CPT 93644 is specific to subcutaneous ICDs, not traditional transvenous ICDs (which use 93289, 93295, or 93296)
Impact: Prevents denials due to incorrect code selection; wrong code could result in $100+ payment difference or complete claim rejection
Document all components: device interrogation, stored data review, sensing assessment, detection evaluation, and any shock testing performed
Impact: Complete documentation supports medical necessity and reduces audit risk; missing elements can trigger recoupment of full $183.08 payment
Bill globally (without modifiers) when both technical and professional components are performed by the same entity in the same setting
Impact: Ensures full $183.08 reimbursement; splitting components unnecessarily reduces total payment by 10-15%
Do not bill 93644 with remote monitoring codes (93298) on the same date of service; these represent different monitoring modalities
Impact: Prevents bundling denials and potential recovery actions; codes are mutually exclusive per NCCI edits
Ensure medical necessity is documented for frequency of evaluations; Medicare typically covers routine checks every 90 days minimum
Impact: More frequent evaluations require symptom-based justification to avoid denials; denied claims lose full $183.08 payment
Verify device manufacturer and model in documentation matches S-ICD systems; currently limited to specific approved devices
Impact: Auditors verify device type against implant records; mismatched documentation can trigger denials and potential fraud investigation
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