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FDA 510(k) Applications Submitted by CARDINAL SPINE, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100698
03/11/2010
STCC
CARDINAL SPINE, LLC
K142030
07/25/2014
STGC-LORDOTIC
CARDINAL SPINE, LLC
K121176
04/18/2012
STGC
CARDINAL SPINE, LLC
K152568
09/09/2015
C-VBR
CARDINAL SPINE, LLC
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