Topera said a new backer, New Enterprise Assoc., led a $25 million Series C round first reported by MassDevice.com last month, with an unnamed "strategic industry partner" joining the round.
The San Diego, Calif.-based startup, which came out of stealth mode at the Heart Rhythm Society meeting last year, won 510(k) clearance from the FDA for its RhythmView 3D mapping system to treat patients with cardiac rhythm disorders by targeting treatment on electrical "hot spots" in the heart.
Yesterday Topera said it plans to use some of the proceeds from the round to back its plans to commercialize the device next year in the U.S. and Europe, according to a press release.
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"We are pleased to partner with this experienced group of investors as we continue our mission to help clinicians obtain information about the sources sustaining complex arrhythmias to significantly improve long-term patient outcomes while reducing costs to providers and the healthcare system," CEO Edward Kerslake said in prepared remarks.
The round, 1st reported by MassDevice.com March 18, closed March 15.
Topera originally unveiled the highly anticipated results of its Confirm study at the Heart Rhythm Society’s annual meeting in Boston in May 2012, touting a 100% success rate. In July, the company released other results from the trial in which researchers said they were able to "shut down atrial fibrillation or very significantly slowed it in 86% of patients in an average of only 2.5 minutes."
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