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FDA 510(k) Applications Submitted by ISOTIS NV
FDA 510(k) Number
Submission Date
Device Name
Applicant
K010840
03/21/2001
SYNPLUG
ISOTIS NV
K000587
02/22/2000
SHUTTLE STOP
ISOTIS NV
K061880
07/03/2006
ACCELI DBM FAMILY PRODUCTS, 0.5CC, 1CC, 2.5CC, 5CC, 10CC, 15CC, 30CC
ISOTIS NV
K060306
02/07/2006
ACCELL CONNEXUS DEMINERALIZED BONE MATRIX PUTTY
ISOTIS NV
K060332
02/09/2006
ORTHOBLAST II DBM DEMINERALIZED BONE MATRIX PASTE AND PUTTY
ISOTIS NV
K041344
05/20/2004
OPEN BORE SYRINGE
ISOTIS NV
K030131
01/14/2003
OSSATURA BCP BONE VOID FILLER
ISOTIS NV
K031813
06/12/2003
OSSATURA DENTAL
ISOTIS NV
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