Orthovita, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
FDA 510(k) cleared devices by Orthovita, Inc. Orthopedic ✕
15 devices
Cleared
May 02, 2017
Vitoss Bioactive (BA) Injectable
Orthopedic
131d
Cleared
Oct 06, 2016
HydroSet XT
Orthopedic
134d
Cleared
Feb 12, 2016
Vitoss BiModal Bone Graft Substitute Foam Strip
Orthopedic
57d
Cleared
Apr 01, 2014
IMBIBE NEEDLE
Orthopedic
42d
Cleared
Feb 07, 2011
VITOSS BA BIMODAL BIOACTIVE BONE GRAFT SUBSTITUTE
Orthopedic
102d
Cleared
Jan 25, 2011
ORTHOVITA PEEK SPACER
Orthopedic
274d
Cleared
Oct 27, 2010
FM-02 BONE GRAFT SUBSTITUTE
Orthopedic
54d
Cleared
Jun 05, 2009
CORTOSS BONE AUGMENTATION MATERIAL
Orthopedic
507d
Cleared
Nov 06, 2008
VITOSS BONE GRAFT SUBSTITUTE, BONE GRAFT SUBSTITUTE FILLED CANISTER, FOAM &...
Orthopedic
27d
Cleared
Jun 17, 2008
VITOSS BIOACTIVE FOAM PACK BONE GRAFT SUBSTITUTE
Orthopedic
26d
Cleared
Sep 18, 2007
VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE
Orthopedic
43d
Cleared
Dec 19, 2003
VITOSS SCAFFOLD FOAM BONE GRAFT MATERIAL
Orthopedic
148d
Cleared
Dec 08, 2003
ENDOSKELETON TA VERTEBRAL BODY REPLACEMENT
Orthopedic
90d
Cleared
Nov 05, 2003
VITOSS-FILLED CARTRIDGE
Orthopedic
117d
Cleared
Aug 29, 2003
VITOSS SCAFFOLD SYNTHETIC CANCELLOUS BONE VOID FILLER
Orthopedic
25d