FDA 510(k) Applications Submitted by INCITE INNOVATION LLC

FDA 510(k) Number Submission Date Device Name Applicant
K130306 02/07/2013 INCITE ANCHORED CERVICAL INTERBODY DEVICE INCITE INNOVATION LLC
K122008 07/09/2012 INCITE ANCHORED CERVICAL INTERBODY (ACI) FUSION DEVICE INCITE INNOVATION LLC
K093808 12/11/2009 INCITE INNOVATION STAND ALONE INTERBODY FUSION DEVICE INCITE INNOVATION LLC


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