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CPT 0547U: Neurofilament Light Plasma Quantitative Assay
CPT code 0547U denotes a Proprietary Laboratory Analyses (PLA) test for measuring neurofilament light chain (NfL) in plasma using a chemiluminescent enzyme immunoassay. As a PLA code, 0547U is tied to a single test produced by specific manufacturers (Neurocode USA Inc. and Fujirebio Diagnostics Inc.), and it standardizes reporting for quantitative NfL results. Nationally, NfL testing has growing clinical relevance as a blood-based biomarker for neuronal injury and neurodegeneration, influencing diagnostic pathways and monitoring strategies across neurology practices.
Key payers included in this analysis are Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. The publication provides readers with an overview of coverage and billing considerations for 0547U, typical sites of service, and the clinical context for ordering plasma NfL testing. Readers will find benchmarks and policy-relevant summaries where available, clinical background on the assay and its intended use, and practical billing metadata such as common modifier usage. Data not provided in the input (including specific coverage policies, reimbursement rates, associated taxonomies, ICD-10 mappings, and related codes) are noted as not available in the input.
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Billing Code Overview
CPT code 0547U is a Proprietary Laboratory Analyses (PLA) code that applies exclusively to a single laboratory test: the Neurofilament Light Blood Test offered by Neurocode USA Inc. and Fujirebio Diagnostics Inc. The test quantitatively measures neurofilament light chain (NfL) concentration in plasma using a chemiluminescent enzyme immunoassay technique. Results are reported as numeric values reflecting NfL levels, used as a biomarker in neurological assessment.
Service Type: Proprietary laboratory blood test (plasma NfL quantification)
Typical Site of Service: Clinical laboratory or reference diagnostic laboratory; specimen collection in outpatient clinics or phlebotomy centers.