Summary & Overview
HCPCS C9122: Mometasone Furoate Sinus Implant, 10 mcg
HCPCS Level II code C9122 denotes a mometasone furoate sinus implant, 10 micrograms (Sinuva), an implantable corticosteroid indicated for prolonged local treatment within the sinonasal cavity. As a device-based intranasal therapy, this code matters nationally because it represents an alternative to repeated systemic or topical therapies for chronic sinus conditions requiring localized steroid delivery. Coverage policies and payment rates for implantable sinus therapies can affect access to this option across outpatient and ambulatory settings.
Key payers referenced include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical context for the implant, typical sites of service, and what to expect in payer engagement. The publication outlines benchmark considerations, common billing modifiers and coding contexts, and areas where policy updates or coverage criteria commonly influence utilization. Information on associated billing practice elements such as service line classification and common claim modifiers is provided where available; if specific payer policy details are absent, the report notes that data are not available in the input. This summary equips billing managers, revenue cycle staff, and clinical leaders with the essentials needed to identify the code, understand its clinical purpose, and anticipate payer interactions on a national scale.
Billing Code Overview
HCPCS Level II code C9122 represents a mometasone furoate sinus implant, 10 micrograms (Sinuva). This device-based therapy delivers localized corticosteroid directly to the sinonasal cavity.
Service Type: Sinus implant / intranasal local drug delivery
Typical Site of Service: Otolaryngology clinic, ambulatory surgery center, or outpatient procedure setting
Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A 45-year-old adult with a history of chronic rhinosinusitis with nasal polyposis presents to an otolaryngology clinic for persistent unilateral nasal obstruction, recurrent sinus infections, and anosmia despite maximal medical therapy including intranasal corticosteroids and a trial of systemic steroids. Nasal endoscopy demonstrates recurrent polypoid disease localized to the ostiomeatal complex of one side. Imaging (sinus CT) confirms localized maxillary and ethmoid disease. The surgeon elects outpatient placement of a steroid-eluting sinus implant (C9122 — mometasone furoate sinus implant, 10 micrograms, Sinuva) in the office procedure suite under local anesthesia.
Workflow:
-
Pre-procedure evaluation and informed consent obtained by the otolaryngologist.
-
Topical and local anesthesia applied; nasal endoscopy performed to visualize target site.
-
Diseased polyp tissue partially debulked as needed using microdebrider or suction cautery (separate CPT code) to create a receptive cavity for the implant.
-
Steroid-eluting implant
C9122is placed endoscopically into the sinus cavity (typically the ethmoid or maxillary space) to deliver localized corticosteroid therapy over weeks to months. -
Post-placement endoscopic confirmation of implant position; brief observation in the clinic; discharge with post-procedure instructions and follow-up visit scheduled for endoscopic assessment and potential implant removal if indicated.
Typical site of service: outpatient otolaryngology clinic or ambulatory surgery/office-based procedure room. Typical patient scenario: adults with recurrent sinonasal polyposis or focal recurrent inflammatory disease not controlled with standard medical therapy who are candidates for localized corticosteroid implant therapy.