FDA 510(k) Applications Submitted by PETER ALLAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K091302	05/04/2009	INTEGRA MOZAIK AND OS MOLDABLE MORSELS	INTEGRA LIFESCIENCES CORPORATION
K031919	06/23/2003	EBI XFIX DFS SYSTEM	EBI, L.P.
K092388	08/05/2009	DURAGEN PLUS DURAL REGENERATION MATRIX- SPINAL MATRIX, MODEL DP2013SM, INTEGRA SPINAL MEND DURAL REGENERATION MATRIX, MO	INTEGRA LIFESCIENCES CORPORATION
K072207	08/08/2007	DURAGEN XS DURAL REGENERATION MATRIX	INTEGRA LIFESCIENCES CORP.
K052239	08/17/2005	EBI DYNAFIX VISION FOOTPLATE SYSTEM	EBI, L.P.
K042237	08/18/2004	EBI PERIARTICULAR PLATING SYSTEM	EBI, L.P.