FDA 510(k) Applications Submitted by CEREMED, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120220	01/25/2012	ADAPTAIN SOLUBLE IMPLANT MATERIAL	CEREMED, INC.
K160988	04/08/2016	Biopor, AOC Porous Polyethylene, Cerepor	CEREMED, INC.
K141880	07/11/2014	BIOPOR AOC POROUS POLYETHYLENE, CEREPOR	CEREMED, INC.
K132198	07/16/2013	ADAPTAIN, ADAPTAIN FASTWRAP, ENVELOCK, BIOWAI	CEREMED, INC.
K122561	08/22/2012	ADAPTAIN FASTWRAP, ENVELOCK, GRAFTAIN	CEREMED, INC.
K050440	02/22/2005	AOC BONE WAX, OSTENE, OSTEOTENE, ORTHOSEAL, OSTEOSEAL, CERETENE, MODEL BW-12	CEREMED, INC.
K080507	02/25/2008	AOC POROUS POLYETHYLENE, AOC POROUS HDPE, AOC POROUS POLYETHYLENE SURGICAL IMPLANT	CEREMED, INC.
K051293	05/18/2005	CRANION CRANIAL FIXATION SYSTEM; FIXLOCK; CRANIAL SOLUTIONS; CEREMED FIXATION SYSTEM	CEREMED, INC.
K081531	06/02/2008	AOC SOLUBLE IMPLANT MATERIAL	CEREMED, INC.
K102071	07/23/2010	OSTENE CT, AOC CT, OSTEOTENE, CERETENE	CEREMED, INC.
K062280	08/07/2006	OSTENE, AOC, OSTEOTENE, CERETENE, CEREPOR, APTENE, APATENE AND ACTIPASTE	CEREMED, INC.
K082245	08/07/2008	AOC, OSTENE, AOC IMPLANT MATERIAL, CERETENE, OSTENE LUBE, AOC-LV	CEREMED, INC.
K082491	08/28/2008	OSTENE CT SOLUBLE BONE HEMOSTASIS IMPLANT MATERIAL, AOC CT, AOC, OSTENE, OSTEOTENE & CERETENE	CEREMED, INC.
K052528	09/14/2005	AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE	CEREMED, INC.
K103047	10/15/2010	CERETENE SOLUBLE IMPLANT MATERIAL	CEREMED, INC.
K043133	11/12/2004	AOC POROUS POLYETHYLENE, AOC POROUS HDPE, AOC POROUS POLYETHYLENE SURGICAL IMPLANT, CEREPOR	CEREMED, INC.