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FDA 510(k) Applications Submitted by ANDREINA ANGIE IDE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030208
01/21/2003
IMBIBE II SYRINGE
ORTHOVITA, INC.
K032409
08/04/2003
VITOSS SCAFFOLD SYNTHETIC CANCELLOUS BONE VOID FILLER
ORTHOVITA, INC.
K023074
09/16/2002
IMBIBE BONE MARROW ASPIRATION SYRINGE
ORTHOVITA, INC.
K032130
07/11/2003
VITOSS-FILLED CARTRIDGE
ORTHOVITA, INC.
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