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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