FDA 510(k) Applications Submitted by ANN-CHRISTINE PROVOOST

FDA 510(k) Number Submission Date Device Name Applicant
K090871 03/30/2009 CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12 BONESUPPORT AB
K062478 08/24/2006 CLAVIS MEDTRONIC A/S
K073316 11/26/2007 CERAMENT BONE VOID FILLER, MODEL A0210 BONESUPPORT AB


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