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Published on 7/13/2006 in the Prospect News Biotech Daily.

Elekta gets OK for treatment planning system for Leksell Gamma Knife Perfexion

By E. Janene Geiss

Philadelphia, July 13 - Elekta said Thursday that the Food and Drug Administration recently approved the 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 said it expands the Leksell Gamma Knife product line with a 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 and neck regions, according to a company news release.

Elekta is a Stockholm, Sweden, medical technology group that provides services for cancer and brain disorders.


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