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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact