FDA 510(k) Applications Submitted by TADEUSZ WELLISZ

FDA 510(k) Number Submission Date Device Name Applicant
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.
K091636 06/04/2009 OSTENE CT, AOC CT, OSTEOTENE, CERETENE 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.
K070093 01/10/2007 OSTENE, AOC, OSTEOTENE, CERETENE, CEREPOR, APTENE, APATENE, ACTIPASTE CEREMED INC.


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