FDA 510(k) Applications Submitted by Ami Akallal-Asaad

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
K211323	04/30/2021	ASTRA 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
K211935	06/22/2021	ORIO-Ti Intervertebral Body Fusion Cage System	SpineCraft, LLC
K132603	08/20/2013	APEX SPINE SYSTEM	SPINECRAFT LLC
K062513	08/28/2006	APEX SPINE SYSTEM	SPINECRAFT, INC.
K102488	08/31/2010	APEX SPINE SYSTEM W/ COCR RODS	SPINECRAFT LLC
K092825	09/11/2009	APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHER	SPINECRAFT, INC.
K223273	10/24/2022	ASTRA Spine System	SpineCraft, LLC
K223301	10/27/2022	ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments System	SpineCraft, LLC
K103505	11/29/2010	ALTUM ANTERIOR CERVICAL PLATE	SPINECRAFT LLC
K143683	12/24/2014	APEX-DL Spine System	SPINECRAFT LLC