FDA 510(k) Applications Submitted by HEATHER GUERIN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K100089	01/12/2010	SYNTHES T-PAL SPACER	SYNTHES SPINE
K120275	01/30/2012	SYNTHES ACIS/VERTEBRAL SPACER CR	SYNTHES (USA) LLC
K120838	03/20/2012	SYNTHES MATRIX SYSTEM	SYNTHES SPINE
K120928	03/27/2012	SYNTHES MATRIX SYSTEM	SYNTHES SPINE
K111048	04/15/2011	SYNTHES SCOUT TACK FIXATION	SYNTHES SPINE
K111358	05/16/2011	SYNTHES USS	SYNTHES SPINE
K131792	06/18/2013	SYNTHECEL DURA REPAIR, SYNTHECEL DURA ONLAY	SYNTHES INC
K113044	10/12/2011	SYNTHES MIRS	SYNTHES SPINE
K113149	10/24/2011	SYNTHES USS CONNECTORS	SYNTHES SPINE
K103320	11/12/2010	SYNTHES XRL	SYNTHES SPINE CO.LP
K093668	11/27/2009	SYNTHES MATRIX MIS RODS	SYNTHES (USA)
K103558	12/02/2010	SYNTHES SCOUT VESSEL GUARD	SYNTHES SPINE