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FDA 510(k) Applications Submitted by JOHN KIRWAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130306
02/07/2013
INCITE ANCHORED CERVICAL INTERBODY DEVICE
INCITE INNOVATION LLC
K150913
04/06/2015
INCITE ANCHORED CERVICAL INTERBODY DEVICE
INCITE INNOVATION
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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