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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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