Osteotech, Inc. - FDA 510(k) Cleared Devices
24
Total
21
Cleared
0
Denied
Osteotech, Inc. has 21 FDA 510(k) cleared orthopedic devices. Based in San Mateo, US.
Historical record: 21 cleared submissions from 1985 to 2008.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
24 devices
Cleared
Oct 16, 2008
GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM...
Orthopedic
37d
Cleared
Jul 22, 2008
PLEXUR M
Orthopedic
83d
Cleared
Apr 21, 2008
PLEXUR-P
Orthopedic
56d
Cleared
Mar 03, 2008
PLEXUR M
Orthopedic
90d
Cleared
Feb 07, 2007
PLEXUR P
Orthopedic
209d
Cleared
Jan 03, 2006
GRAFTON DBM
Dental
238d
Cleared
Dec 16, 2005
GRAFTON DBM
Orthopedic
220d
Cleared
Dec 16, 2005
GRAFTCAGE TLX
Orthopedic
168d
Cleared
Dec 05, 2005
VIAGRAF DBM PASTE
Orthopedic
381d
Cleared
Dec 01, 2005
GRAFTCAGE ACX
Orthopedic
29d
Cleared
Nov 30, 2005
GRAFTON PLUS DBM PASTE
Dental
426d
Cleared
Nov 23, 2005
GRAFTON PLUS DBM PASTE
Orthopedic
384d
Cleared
Oct 16, 2001
VBR
Orthopedic
90d
Cleared
Jan 04, 2001
VERTEBRAL BODY REPLACEMENT
Orthopedic
86d
Cleared
Nov 24, 2000
VERSALINK TITANIUM ROD-TO-ROD COUPLERS
Orthopedic
24d
Cleared
Nov 19, 1999
VERSALOK LOW BACK FIXATION SYSTEM
Orthopedic
84d
Cleared
Jul 23, 1999
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
Orthopedic
77d
Cleared
Jan 08, 1998
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
Orthopedic
90d
Cleared
Jun 18, 1997
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
Orthopedic
72d
Cleared
Feb 09, 1996
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
Orthopedic
88d
Cleared
Jun 22, 1995
OSTEOTECH NAVICULAR AND CANCELLOUS CANNULATED SCREWS
Orthopedic
129d
Cleared
May 31, 1995
OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK
General & Plastic Surgery
42d
Cleared
Oct 13, 1988
ALLOPREP SYSTEM
Pathology
85d
Cleared
Oct 07, 1985
OSTEOGRAF 2040 OSTEOGRAF 4060
Dental
140d