US Edition
Philips receives FDA 510(k) clearance for image-guided navigation system for prostate cancer - Interventional News
Summary by Interventional News
This story is only covered by news sources that have yet to be evaluated by the independent media monitoring agencies we use to assess the quality and reliability of news outlets on our platform. Learn more here.1 Articles
1 Articles
Philips receives FDA 510(k) clearance for image-guided navigation system for prostate cancer - Interventional News
Philips UroNav Philips has announced the FDA 510(k) clearance of the latest Philips UroNav system. In a recent press release made by the company, it states that the system includes a new advanced annotation workflow that supports clinicians during focal therapy procedures, helping deliver more precise, minimally invasive care. “We’re entering a new era of precision prostate cancer care. Philips’ integrated focal therapy platform unifies imaging,…
Coverage Details
Total News Sources1
Leaning Left0Leaning Right0Center0Last UpdatedBias DistributionNo sources with tracked biases.
Bias Distribution
- There is no tracked Bias information for the sources covering this story.
Factuality
To view factuality data please Upgrade to Premium
