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FDA Device Clearances: Percutaneous Dual Rod Accepting Polyaxial Screw, Light Therapy Device, Cystic
Link ID 4093
Title FDA Device Clearances: Percutaneous Dual Rod Accepting Polyaxial Screw, Light Therapy Device, Cystic
Url http://www.medscape.com/viewarticle/571604?src=rss
Description The FDA has granted 510(k) clearance for a percutaneous dual rod-accepting polyaxial screw (Silverbolt Percutaneous Multi-Level Rod System), a handheld over-the-counter light therapy device (Omnilux New-U), and a cystic fibrosis molecular test (InPlex CF). Medscape Medical News
Category Articles > Business of Medicine
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Date Mar 20, 2008
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