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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