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                              ELEKTA RECEIVES U.S. REGULATORY APPROVAL FOR TREATMENT PLANNING ON LEKSELL GAMMA KNIFE® PERFEXION™

                              July 13, 2006
                              PRESS RELEASE
                              Stockholm, Sweden, July 13, 2006

                              On July 5, the U.S. Federal Drug Administration (FDA) announced a 510(k) pre-market clearance for Leksell GammaPlan® PFX™, the treatment planning system developed for Leksell Gamma Knife® Perfexion™.

                              By the ongoing market introduction of Leksell Gamma Knife Perfexion, Elekta expands the Leksell Gamma Knife® product line with a completely new system that takes stereotactic radiosurgery to the next level and provides a radiosurgical platform for further refinement and expansion of procedures in the brain, cervical spine and head & neck regions. Leksell Gamma Knife Perfexion is pending 510(k) clearance from the FDA.“Leksell GammaPlan PFX is a vital part of Elekta’s brand new platform for stereotactic radiosurgery, providing unmatched ease-of-use and reaping the benefits of the highly innovative design of Leksell Gamma Knife Perfexion”, says Vincent Denot, Elekta’s Product Manager for Leksell GammaPlan. “This 510(k) pre-market clearance from FDA is an important milestone in the Perfexion project and yet another such event that is occurring exactly according to plan”, Denot concludes.******

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                              Important Safety Information: Radiation therapy is not appropriate for all patients. Radiation treatments may cause side effects that can vary depending on the part of the body being treated. In some patients, they can be severe. Treatment sessions may vary in complexity and time. Refer to individual product labeling (instructions for use) for more complete information on product safety and effectiveness for its intended use.

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                              Important Safety Information: Radiation therapy is not appropriate for all patients. Radiation treatments may cause side effects that can vary depending on the part of the body being treated. In some patients, they can be severe. Treatment sessions may vary in complexity and time. Refer to individual product labeling (instructions for use) for more complete information on product safety and effectiveness for its intended use.