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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.
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