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