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FDA clears NOMOS' brachytherapy planning system:

This article was originally published in Clinica

Executive Summary

NOMOS has received US FDA 510(k) clearance to market its ultrasound-guided brachytherapy planning system for use in the treatment of prostate cancer. The stand-alone Ultraseed device, which provides treatment planning tools such as real-time image capture, seed optimisation and automatic seed sorting for post-planning, allows doctors to plan and deliver brachytherapy treatments accurately and quickly, said the Sewickley, Pennsylvania-based company.

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