Osteobiologics, Inc. - FDA 510(k) Cleared Devices
9
Total
8
Cleared
0
Denied
Osteobiologics, Inc. has 8 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Historical record: 8 cleared submissions from 2002 to 2005. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Osteobiologics, Inc. Filter by specialty or product code using the sidebar.
9 devices
Cleared
Oct 25, 2005
OCT (OSTEOCHONDRAL TRANSPLANT) COMPREHENSIVE SYSTEM
Orthopedic
126d
Cleared
Jun 17, 2005
POLYGRAFT BGS
Orthopedic
388d
Cleared
Jan 07, 2005
TRUGRAFT BGS SYRINGE, MODEL 600-041
General Hospital
52d
Cleared
Dec 17, 2004
POLYGRAFT BGS
Orthopedic
340d
Cleared
Aug 16, 2004
POLYGRAFT TCP GRANULES, CUBES, BLOCKS, PLUGS, WEDGES, MODELS 600-023-XX,...
Orthopedic
264d
Cleared
Oct 02, 2003
IMMIX PLASTIFILM
General & Plastic Surgery
34d
Cleared
Jul 17, 2003
POLYGRAFT BONE GRAFT SUBSTITUTE
Orthopedic
170d
Cleared
Mar 14, 2003
IMMIX THIN FILM, MODELS: PSS-004-S, PSS-004-SP, PSS-004-M, PSS-004-MP,...
General & Plastic Surgery
84d
Cleared
Jan 11, 2002
ACTAEON PROBE
Orthopedic
87d