CPT 81507: Assay-Specific Cell-Free DNA ScreeningAssay-Specific Cell-Free DNA Screening
81507 describes cell-free DNA screening for the common fetal trisomies (21, 18, and 13) performed by one laboratory's specific proprietary method. Clinically it is the same NIPT service as 81420; the code differs because it is assigned to a particular assay rather than to the service category. The performing lab bills it, and a lab reports 81507 or 81420, never both.
When to use 81507
The ordering practice never chooses between 81507 and 81420; the lab does, based on which assay it runs and which code it holds. What the practice should know is that the two codes are interchangeable at the policy level: prior-auth requirements, coverage criteria, and denial patterns track the service, not the code number. If a payer's NIPT policy lists 81420, it almost always lists 81507 in the same paragraph. The practice-side work is identical: indication, diagnosis code, prior auth, counseling.
Documentation checklist
Documentation lives on the practice side even though the claim goes out under the lab's NPI. The record that supports an 81507 claim is the same record that supports 81420.
Global package rules
Like all prenatal lab work, this screen sits outside the global OB package and never touches the 59400 claim. It is a clinical laboratory service priced on the Clinical Laboratory Fee Schedule rather than the Medicare Physician Fee Schedule, so no MPFS fee table appears on this page. One practical wrinkle unique to assay-specific codes: if the practice obtains prior authorization under 81420 but the lab bills 81507, some payers treat the auth as mismatched. Confirm with the lab which code it reports before requesting the auth. CMS