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1. Storming the Gates: Sentinel Lymph Node Targeting & Assessment

   ... referred to as Lymphoseek (Navidea), was approved by the FDA in March. Wallace has been instrumental in major U.S. clinical trials ... use in metastases of the breast and in cases of melanoma. FDA approval was based on two clinical trials involving 332 patients with ...

   mrivera - 2013-05-21 12:00

2. Imaging Parkinson’s: The Search for Biomarkers

   ... use since being approved in Europe in 2000 and by the FDA in 2011. DAT scans zero in on the major dopamine pathway from the ...

   mrivera - 2013-05-21 11:02

3. Battlefield Innovations Boost Medical Care from Baghdad to Boston

   ... swing joint/locked leg prosthetic model. Also in the FDA pipeline is the experimental concept of osseointegration. “Instead of a ...

   mrivera - 2013-05-06 09:19

4. Patient Management: When ICD Leads Go Awry

   ... report all lead dysfunction to the manufacturers and to the FDA. He also suggests returning all damaged, extracted leads to the ...

   mrivera - 2013-05-02 09:36

5. Do the Right Things: Top 10 Ways to Provide Strategic Leadership

   ... safety and clinical effectiveness of their products prior to FDA review. "A healthcare technology leader is someone who can think outside ...

   dcaparco - 2013-04-18 17:50

6. Florbetapir: Alzheimer’s Imaging Inches Into Practice

   ... for radiologists interpreting florbetapir scans delayed FDA approval of florbetapir one year. The agency wanted Lilly to establish a ...

   mrivera - 2013-03-04 13:07

7. Xarelto approved in Europe for post-ACS treatment

   ... reduction in mortality risk.” In the U.S., the FDA has given a cold shoulder to rivaroxaban for the reduction of the risk ...

   cstuart - 2013-05-24 16:47

8. Lifesaving combo of CT + 3D printing repairs baby’s airway

   ... Green and his UM colleagues consulted with the FDA and received approval under the emergency-use exemption to implant a ...

   egodt - 2013-05-24 14:19

9. FDA makes Zilver stent Class I recall

   The FDA has issued a Class I recall of Zilver PTX Drug-Eluting Peripheral Stent. ...

   cstuart - 2013-05-24 11:25

10. Nephosity’s MobileCT Viewer Receives FDA 510(k) Clearance for Diagnostic Image Viewing on iPads

    ... from the United States Food and Drug Administration (FDA) for their MobileCT Viewer, a software application for diagnostic image ... lowers costs, engages patients, and improves care. This FDA 510(k) clearance reaffirms the quality and safety of MobileCT Viewer, and ...

    egodt - 2013-05-23 16:34

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