Philips Receives FDA 510(k) Clearance for Advanced Image-Guided Navigation Technology in Prostate Cancer Care

Reuters
07-23
Philips Receives FDA 510(k) Clearance for Advanced Image-Guided Navigation Technology in Prostate Cancer Care

Koninklijke Philips NV has announced a significant advancement in prostate cancer care with the FDA 510(k) clearance for its latest image-guided navigation technology, Philips UroNav. This approval marks a major step in supporting prostate cancer diagnosis by offering clinicians more precise guidance, thereby enhancing patient care. The upgraded UroNav system integrates pre-procedural MRI with real-time ultrasound imaging, providing a dynamic and comprehensive view of the targeted area for minimally invasive procedures. Additionally, it includes a new advanced annotation workflow aimed at improving the accuracy of focal therapy procedures. This development is part of Philips' broader effort to streamline complex workflows in prostate cancer care, equipping clinicians with the necessary tools to deliver better and more precise treatment options.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Royal Philips NV published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW1001119272-en) on July 23, 2025, and is solely responsible for the information contained therein.

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