Summary & Overview
HCPCS L7402: Addition to Upper Extremity Prosthesis, Shoulder Disarticulation
HCPCS Level II code L7402 denotes an ultralight-material addition to an upper extremity prosthesis for shoulder disarticulation or interscapular thoracic amputations. This prosthetic component supports restoration of arm function for high-level amputations where lightweight, durable materials such as titanium or carbon fiber are preferred to improve wearability and mobility. Nationally, prosthetic components for shoulder-level fittings are a specialized segment of durable medical equipment with implications for device availability, clinician expertise, and payer coverage policies.
Key payers in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of the clinical application and setting for L7402, plus what to expect from payer coverage patterns and common billing practices. The publication outlines typical service lines and site-of-service considerations, summarizes benchmarks where available, and highlights recent policy considerations affecting prosthetic component authorization and documentation. This resource is intended to inform billing staff, prosthetists, and policy analysts about the role of L7402 in prosthetic care delivery and reimbursement workflow.
Data not available in the input: associated taxonomies, ICD-10 diagnoses, related codes, and specific payer coverage limits or rates.
Billing Code Overview
HCPCS Level II code L7402 describes an addition to an upper extremity prosthesis for shoulder disarticulation/interscapular thoracic fittings constructed from ultralight material (titanium, carbon fiber or equal). This component is intended to be integrated into a prosthetic system to restore upper-limb function for individuals with shoulder-level amputations.
Service type: Prosthetic component fabrication and fitting
Typical site of service: Prosthetics and orthotics clinics, specialty prosthetic fabrication labs, and outpatient rehabilitation settings
Clinical & Coding Specifications
Clinical Context
A 42-year-old male with a prior traumatic shoulder disarticulation presents to a prosthetics clinic for fitting of an upper extremity prosthetic system. The patient requires an ultralight structural addition to a shoulder disarticulation/interscapular thoracic prosthesis to reduce weight and improve function. The clinical workflow includes a consultation with a prosthetist and physician for medical necessity documentation, measurement and casting of the residual thoracic/shoulder anatomy, fabrication of the ultralight component (titanium or carbon fiber), fitting and alignment, and follow-up visits for adjustments and training in donning/doffing and functional use. Documentation includes the prosthetic prescription, description of the ultralight material used, justification for addition versus standard componentry, itemized device parts, and functional goals (e.g., improved prosthesis endurance and shoulder harness comfort). Typical sites of service are outpatient prosthetics clinics, hospital-based prosthetics departments, or specialized orthotics and prosthetics (O&P) facilities that handle upper extremity prosthetic fabrication and fittings.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
22 | Increased procedural services | Use when additional work or complexity beyond usual is documented (e.g., extensive modification, complex fitting). |