Medtech giants jockeyed for attention to their coronary catheterization products at the 26th Transcatheter Cardiovascular Therapeutics (TCT) meeting held this week in Washington, D.C., according to a report on bidnessetc.com and company announcements.
Minneapolis-based Medtronic had lots to talk about. The Food and Drug Administration gave 510(k) approval last week to its NC Euphora Noncompliant Balloon Dilatation Catheter for use in heart replacement surgeries. The company received the CE Mark to market the device in Europe in May.
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