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Home » Biotronik scores win as FDA gives green light to PK Papyrus stent
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Biotronik scores win as FDA gives green light to PK Papyrus stent

Sep. 18, 2018
By Liz Hollis
For the first time in nearly two decades, the FDA has approved a device intended to treat acute coronary artery perforations. The PK Papyrus covered coronary stent system, from Biotronik Inc., of Lake Oswego, Ore., won approval under a humanitarian device exemption for use in the emergency treatment of tears in the blood vessels of the heart.
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