Intracorneal ring segments (ICRS) are micro-thin prescription inserts which were previously used as a form of refractive surgery in the treatment of low levels of myopia or nearsightedness, but has recently received FDA approval for keratoconus. ICRS are thin plastic, semi-circular rings inserted into the mid layer of the cornea. When inserted in the keratoconus cornea they flatten the cornea, changing the shape and location of the cone. The placement of Intacs remodels and reinforces the cornea, eliminating some or all of the irregularities caused by keratoconus in order to provide improved vision. This can improve uncorrected vision, however, depending on the severity of the KC, glasses or contact lenses may still be needed for functional vision.
FDA Approval Intacs were approved under a Humanitarian Device Exemption (HDE) by the FDA in July 2004, allowing Intacs to be used for treating keratoconus. As part of the HDE approval, Addition Technology, the manufacturer of Intacs, has implemented an extensive training program in which each surgeon will be required to participate. What is a Humanitarian Device Exemption (HDE)? The humanitarian device regulations were first established in October 1994. Humanitarian Use Devices (HUDs) are medical devices specially designated by the FDA for use in the treatment of fewer than 4000 patients per year with rare medical conditions. CPT Code is: Category III CPT code 0099T Intacs received a Category III CPT code 0099T from the American Medical Association. Category III CPT codes are codes to designate emerging technologies and are not assigned a value. It is up to the insurance company to determine the amount to be paid.
ICRS Surgery Procedure
For more information go to: www.intacsforkeratoconus.com