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» Atricure probes underpenetrated AF market with latest FDA clearance
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Atricure probes underpenetrated AF market with latest FDA clearance
April 13, 2016
By
Amanda Pedersen
Flexibility is the key differentiator of Atricure Inc.'s newest FDA-cleared device. The company launched the Cryoform cryoablation probe in Europe last year under a CE mark and now has an FDA 510(k) clearance for the U.S. market.
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