FDA 510(k) Applications Submitted by CHRISTINE NASSIF

FDA 510(k) Number	Submission Date	Device Name	Applicant
K022199	07/05/2002	ENDIUS ATAVI SYSTEM	ENDIUS, INC.
K070367	02/08/2007	ENDIUS TITLE 2 POLYAXIAL SPINAL SYSTEM	ENDIUS, INC.
K060683	03/15/2006	ENDIUS MINIT POSTERIOR CERVICAL AND UPPER THORACIC FIXATION SYSTEM	ENDIUS, INC.
K060990	04/10/2006	ENDIUS TITLE 2 POLY AXIAL SPINAL SYSTEM	ENDIUS, INC.
K191101	04/25/2019	Kendall NPWT Incision Management Dressing Kit	Cardinal Health
K061345	05/15/2006	MODIFICATION TO ENDIUS ATAVI SYSTEM	ENDIUS, INC.
K021748	05/28/2002	ENDIUS ATAVI SYSTEM	ENDIUS, INC.
K021881	06/07/2002	ENDIUS TITLE SPINAL FIXATION SYSTEM	ENDIUS, INC.
K041808	07/06/2004	ENDIUS TITLE 2 POLYAXIAL SPINAL SYSTEM	ENDIUS, INC.
K992487	07/26/1999	MITEK MINI QUICKANCHOR PLUS	MITEK PRODUCTS
K992611	08/04/1999	MITEK ROTATOR CUFF QUICKANCHOR PLUS	MITEK PRODUCTS
K022578	08/05/2002	ENDIUS FLEXTIP BLADE	ENDIUS, INC.
K202217	08/06/2020	Kendall NPWT Incision Management Device	Cardinal Health
K003076	10/03/2000	MITEK CUFFTACK	MITEK PRODUCTS
K072840	10/04/2007	ENDIUS TITLE 2 POLYAXIAL SPINAL SYSTEM	ENDIUS, INC.
K013572	10/29/2001	MITEK BIOCRYL INTERFERENCE SCREWS	MITEK PRODUCTS
K053267	11/23/2005	ENDIUS ATAVI SYSTEM	ENDIUS, INC.
K111062	04/18/2011	APEX KNEE SYSTEM, APEX ALL POLY TIBIA	OMNILIFE SCIENCE INC.
K112779	09/26/2011	APEX MODULAR ACCTABULAR CUP (NOW NAMED APEX INTERFACE ACETABULAR SYSTEM)	OMNLIFE SCIENCE
K112891	09/30/2011	APEX REVISION KNEE SYSTEMS	OMNI LIFE SCIENCE, INC.
K113242	11/02/2011	APEX ARC HIP STEM	OMNILIFE SCIENCE INC.