Summary & Overview
HCPCS C9459: Flutemetamol F-18 Diagnostic PET Dose
HCPCS Level II code C9459 designates flutemetamol F-18 provided as a diagnostic radiopharmaceutical dose (up to 5 millicuries) for PET brain imaging. This agent is used to support visualization of cerebral pathology and is relevant in the diagnostic evaluation of neurodegenerative conditions and other brain disorders where PET amyloid imaging or related physiology-focused studies are indicated. Nationally, radiopharmaceutical codes like C9459 are important for consistent billing, coverage determinations, and tracking utilization of advanced diagnostic imaging.
Key payers included in this analysis are Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of the clinical context for flutemetamol F-18, common sites where the service is delivered, and what to expect in payer coverage conversations. The publication outlines reimbursement benchmarks, typical claim considerations for radiopharmaceuticals, and any recent policy updates affecting HCPCS Level II radiopharmaceutical coding where available. It also summarizes how C9459 fits into imaging service lines and operational workflows for hospitals and outpatient imaging centers.
Data not available in the input for detailed modifiers, associated taxonomies, specific ICD-10 diagnoses, payer-specific coverage rules, and related codes.
Billing Code Overview
HCPCS Level II code C9459 refers to Flutemetamol F-18, a radiopharmaceutical supplied for diagnostic PET imaging, described as "Flutemetamol f18, diagnostic, per study dose, up to 5 millicuries". This service is a diagnostic nuclear medicine imaging agent used to visualize physiological processes in the brain.
Service type: Nuclear medicine diagnostic radiopharmaceutical for PET imaging
Typical site of service: Hospital outpatient departments, imaging centers, and specialized PET clinics
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Clinical & Coding Specifications
Clinical Context
A typical patient is an adult referred for brain amyloid imaging to evaluate suspected Alzheimer disease or other causes of cognitive decline. The patient presents to an outpatient nuclear medicine or PET imaging center. Pre-procedure steps include review of clinical indications (progressive memory loss, MCI, or atypical dementia), obtaining consent, assessment of contraindications (pregnancy, breastfeeding), and verification of the ordering physician’s documentation. On the day of service, an intravenous line is placed, and the radiopharmaceutical C9459 (flutemetamol F18, up to 5 mCi per study dose) is administered. After the recommended uptake period, PET imaging of the brain is performed per facility protocol. Post-procedure, images are processed and interpreted by a qualified nuclear medicine physician or neuroradiologist, and a diagnostic report is transmitted to the referring clinician for correlation with clinical findings and management planning.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the physician interpretation for the PET study separate from technical services provided by the facility. |
TC |