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BioWorld - Friday, June 12, 2026
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TAVR: What it says about FDA and CMS

Feb. 29, 2012
By Mark McCarty
The story has been out for a while about transcatheter aortic valve replacement (TAVR), so maybe it's time to project into the future. Before we head there, however, we should revisit the past. The pivotal event in this story is the drug-eluting stent, a device that gave birth to what FDA's Bram Zuckerman, MD, described as the DES trauma. The DES story is twofold; rapid physician adoption and late-stent thrombosis (LST). FDA saw the rate of adoption as an unruly and harmful stampede because of LST, but...
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Court report: Globus in $1M settlement with FDA for device distribution

Feb. 29, 2012

Product Briefs

Feb. 29, 2012

People in the News

Feb. 29, 2012

MDD's Oncology Extra

Feb. 29, 2012

Financings roundup: Health Care REIT raises $1.1B in public offering

Feb. 29, 2012

HIT roundup: ADI's iCoupler technology to enable Lantronix servers

Feb. 29, 2012

Agreements/contracts: Avedro seeks to option IP assets with Cleveland Clinic

Feb. 29, 2012

Med-Tech Notes: BioNJ to host event at Princeton

Feb. 29, 2012

Ventana gains 510(K) clearance to market image analysis application

Feb. 29, 2012
By Omar Ford
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