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FDA 510(k) Applications Submitted by ANGIE IDE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K011087
04/10/2001
ORTHOVITA PISTON SYRINGE OR IMBIBE BONE MARROW ASPIRATION SYRINGE
ORTHOVITA, INC.
K953337
07/17/1995
BETA HIP PROSTHESIS
ZIMMER, INC.
K954744
10/16/1995
ZCH ALPHA SYSTEM
ZIMMER, INC.
K994337
12/23/1999
VITOSS SCAFFOLD SYNTHETIC CANCELLOUS BONE VOID FILLER
ORTHOVITA CO.
K955473
11/30/1995
GAMMA SYSTEM
ZIMMER, INC.
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