Elekta gets FDA clearance for Monaco 5

Radiation oncology firm Elekta has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its Monaco 5 radiation therapy treatment planning systems.

The latest version consolidates all of Elekta's treatment planning capabilities into a single system, according to the vendor. Monaco now supports the full spectrum of radiotherapy techniques, including volumetric-modulated arc therapy (VMAT), intensity-modulated radiation therapy (IMRT), and 3D conformal radiation therapy, Elekta said.

Monaco 5 is now available for purchase and use in the U.S.

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