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Ark. Code Ann. § 23-86-122

Prior approval process for experimental and investigational surgical products and medical devices — Definition

Acts 2013, No. 464, § 1; 2015, No. 1164, § 6.

(1) As used in this section: “Health carrier” means a: Health maintenance organization;

(2) Hospital medical service corporation; and

(3) Disability insurance company;

(4) “Health carrier” includes a: Self-insured governmental or church plan; and

(5) Third-party administrator that administers or adjusts disability benefits for a disability insurer, hospital medical service corporation, health maintenance organization, self-insured governmental plan, or self-insured church plan; and

(6) “Health carrier” does not include: An automobile insurer paying medical or hospital benefits under § 23-89-202(1) or a self-insured employer health benefits plan; or

(7) A person, company, or organization licensed or registered to issue or that issues an insurance policy or insurance contract in this state as described in §§ 23-62-102 and 23-62-104 — 23-62-107 providing medical or hospital benefits for accidental injury or disability.

(8) A health carrier that excludes or denies coverage for a specific surgical product or medical device approved for marketing by the United States Food and Drug Administration as experimental or investigational, or both, shall develop a process by which a surgeon, before utilizing the surgical product or medical device, may present medical evidence to obtain a review for the individual patient for coverage of the surgical product or medical device.

Current official text: Arkansas General Assembly. Digitized from the UniCourt Code Improvement Commission public-domain capture. Reproduced from public-domain Arkansas statutes; confirm against the official source for the current text. Not legal advice.