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FDA 510(k) Applications Submitted by ELIANE SCHUTTE
FDA 510(k) Number
Submission Date
Device Name
Applicant
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
K040419
02/18/2004
DYNAGRAFT II
ISOTIS ORTHOBIOLOGICS, INC
K041344
05/20/2004
OPEN BORE SYRINGE
ISOTIS NV
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