FDA 510(k) Applications Submitted by SPINECRAFT LLC

FDA 510(k) Number Submission Date Device Name Applicant
K150417 02/18/2015 ASTRA SPINE SYSTEM SPINECRAFT LLC
K110906 03/31/2011 APEX SPINE SYSTEM SPINECRAFT LLC
K181350 05/22/2018 ASTRA-OCT Spine System SpineCraft LLC
K131521 05/28/2013 VELOX ANTERIOR CERVICAL PLATE SYSTEM SPINECRAFT LLC
K132603 08/20/2013 APEX SPINE SYSTEM SPINECRAFT LLC
K102488 08/31/2010 APEX SPINE SYSTEM W/ COCR RODS SPINECRAFT LLC
K103505 11/29/2010 ALTUM ANTERIOR CERVICAL PLATE SPINECRAFT LLC
K143683 12/24/2014 APEX-DL Spine System SPINECRAFT LLC


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