OAR 410-122-0325: Power Wheelchair Base

Edition: Current OARD snapshotEffective: UnknownLast verified: 2026-09-07

Official history and status

Statutory/Other Authority: ORS 413.042 & 414.065

Statutes/Other Implemented: ORS 414.065

History: (I) How long the condition has been present; (II) Clinical progression; (III) Interventions that have been tried and the results; (IV) Past use of walker, manual wheelchair, POV, or PWC and the results. (iv) Physical exam: (I) Weight; (II) Impairment of strength, range of motion, sensation, or coordination of arms and legs; (III) Presence of abnormal tone or deformity of arms, legs, or trunk; (IV) Neck, trunk, and pelvic posture and flexibility; (V) Sitting and standing balance. (v) Functional assessment indicating any problems with performing the following activities including the need to use a cane, walker, or the assistance of another person: (I) Transferring between a bed, chair, and power mobility device; (II) Walking around their home or community including information on distance walked, speed, and balance. (C) The examination must clearly distinguish the client’s abilities and needs within the home and community. (b) The practitioner’s written order received by the DMEPOS provider within 45 days (date stamp or equivalent must be used to document receipt date) after the practitioner’s face-to-face examination. The order must include all of the following elements: (A) Client’s name; (B) Description of the item that is ordered. This may be general (e.g., “power wheelchair” or “power mobility device”) or may be more specific: (i) If this order does not identify the specific type of PWC that is being requested, the DMEPOS provider must clarify this by obtaining another written order that lists the specific PWC that is being ordered and any options and accessories requested; (ii) The items on this clarifying order may be entered by the DMEPOS provider. This subsequent order must be signed and dated by the treating practitioner, received by the DMEPOS provider, and submitted to the authorizing authority, but does not have to be received within 45 days following the face-to-face examination. (C) Date of the face-to-face examination; (D) Pertinent diagnoses/conditions and diagnosis codes that relate specifically to the need for the PWC; (E) Length of need; (F) Practitioner’s signature; (G) Date of practitioner’s signature. (c) For all requested equipment and accessories, the manufacturer’s name, product name, model number, standard features, specifications, dimensions, and options; (d) Detailed information about client-owned equipment (including serial numbers) as well as any other equipment being used or available to meet the client’s medical needs, including how long it has been used by the client and why it cannot be grown (expanded) or modified, if applicable; (e) If the client shall be using the PWC in the home, the DMEPOS provider or practitioner must perform an on-site, written evaluation of the client’s living quarters, prior to delivery of the PWC. This assessment must support that the client’s home can accommodate and allow for the effective use of a PWC. Assessment must include but is not limited to evaluation of physical layout, doorway widths, doorway thresholds, surfaces, counter or table height, accessibility (e.g., ramps), electrical service, etc.; (f) A written document (termed a detailed product description) prepared by the DMEPOS provider and signed and dated by the practitioner that includes: (i) The specific base (HCPCS code and manufacturer name/model) and all options and accessories (including HCPCS codes), whether PA is required or not, that shall be billed separately; (ii) The DMEPOS provider’s charge and the Division fee schedule allowance for each separately billed item; (iii) If there is no Division fee schedule allowance, the DMEPOS provider must enter “not applicable”; (iv)The DMEPOS provider must receive the signed and dated detailed product description from the practitioner prior to delivery of the PWC; (v) A date stamp or equivalent must be used to document receipt date of the detailed product description. (g) Any additional documentation that supports indications of coverage are met as specified in this rule; (h) The DMEPOS provider must keep the above documentation on file; (i) Documentation that the coverage criteria have been met must be present in the client’s medical records and made available to the Division upon request. (5) Reimbursement: (a) Codes specified in this rule shall not be reimbursed for clients residing in nursing facilities; (b) Reimbursement on standard Group 1 and Group 2 wheelchairs without power option (K0813-K0816, K0820-K0829) shall only be made on a monthly rental basis; (c) Rented equipment is considered purchased after thirteen (13) continuous months of rent or the Division fee schedule purchase price or the actual charge from the provider is met, whichever is less. (6) Documentation: (a) For services requiring prior authorization, submit documentation that supports coverage criteria in this rule are met; (b) Documentation that the coverage criteria have been met must be present in the client’s medical record. This documentation and any additional medical information from the DMEPOS provider must be made available to the Division upon request. (7) Procedure codes: (a) The Medicare Pricing, Data Analysis and Coding (PDAC) contractor assists DMEPOS providers and manufacturers in determining which codes shall be used to describe DMEPOS items. See 410-122-0180 Healthcare Common Procedure Coding System (HCPCS) Level II Coding for more information; (b) Refer to the product classification list on the PDAC contractor website for appropriate HCPCS codes. (c) Refer to Table 122-0325. [ED. NOTE: To view attachments referenced in rule text, click here to view rule.]

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Official source: https://secure.sos.state.or.us/oard/