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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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