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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