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Home » Authors » Katie Pfaff

Katie Pfaff

katie.pfaff@clarivate.com
Articles

ARTICLES

Myomo offers robotics industry IPO

June 13, 2017
By Katie Pfaff
Medical robotics company Myomo Inc. goes public with IPO offering of $5 million at $7.50 per share. The Cambridge, Mass., company specializes in mobility devices for the arms and hands.
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Siemens wins FDA OK for molecular imaging for software to enhance tumor comparison

June 12, 2017
By Katie Pfaff

Surefire's transarterial chemoembolic infusion more effective with liver tumors, says study

June 9, 2017
By Katie Pfaff

Hologic brings 3-D method to dense breast cancer detection

June 8, 2017
By Katie Pfaff

Edwards Lifesciences is first in mitral valve repair with FDA approval of Sapien 3

June 7, 2017
By Katie Pfaff
Edwards Lifesciences Corp. won FDA approval for its Sapien 3 transcatheter heart valve device for aortic and mitral valve-in-valve procedures. The Irvine, Calif.-based company leads the way in a burgeoning sector of the market with the expanded indication. The minimally invasive valve procedure device segment for patients who are not indicated for traditional surgery is expected to grow over the next decade, analysts predict. "The global transcatheter heart valve replacement and repair [THVR] market was valued at $1.6 billion in 2015 and is expected to expand at a CAGR of 13.9 percent over the forecast...
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Edwards Lifesciences is first in mitral valve repair with FDA approval of Sapien 3

June 7, 2017
By Katie Pfaff
Edwards Lifesciences Corp. won FDA approval for its Sapien 3 transcatheter heart valve device for aortic and mitral valve-in-valve procedures. The Irvine, Calif.-based company leads the way in a burgeoning sector of the market with the expanded indication. The minimally invasive valve procedure device segment for patients who are not indicated for traditional surgery is expected to grow over the next decade, analysts predict.
Read More

Claret Medical's debris filter used after TAVR is cleared for use by FDA

June 6, 2017
By Katie Pfaff
Claret Medical Inc. won FDA clearance for its Sentinel device to capture debris from a transcatheter aortic valve replacement (TAVR) and reduce risk of stroke. Touted by the Santa Rosa, Calif.-based company as the first of its kind in the U.S., the device blocks microphages, fibrin and cholesterol materials loosened during the procedure which can then travel to the brain.
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Synaptive Medical, CSU seek to define tumors intraoperatively, improve surgical results

June 5, 2017
By Katie Pfaff

Synthetic cartilage maker Hyalex collects $16.3M in series A funding

June 2, 2017
By Katie Pfaff

Ra Medical's laser ablative PAD treatment is now FDA-approved

May 31, 2017
By Katie Pfaff
View All Articles by Katie Pfaff

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