Abbott Spine, Inc. is one of 26090 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Abbott Spine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NEXLINK OCT SYSTEM, MODEL 7000 SERIES, SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS 3308, 3309, 3310), UNIVERSAL CLAMP STAINLESS STEEL SYSTEM
13
Total
13
Cleared
0
Denied
Abbott Spine, Inc. has 13 FDA 510(k) cleared orthopedic devices. Based in Austin, US.
Historical record: 13 cleared submissions from 2005 to 2009.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Abbott Spine, Inc.
13 devices
Cleared
Jun 02, 2009
NEXLINK OCT SYSTEM, MODEL 7000 SERIES
Orthopedic
144d
Cleared
Oct 06, 2008
SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS...
Orthopedic
81d
Cleared
Aug 29, 2008
UNIVERSAL CLAMP STAINLESS STEEL SYSTEM
Orthopedic
80d
Cleared
Jan 30, 2008
ARDIS SPACER
Orthopedic
78d
Cleared
Nov 28, 2007
SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES
Orthopedic
68d
Cleared
Jul 25, 2007
PATHFINDER SYSTEM POLYAXIAL PEDICLE SCREWS
Orthopedic
89d
Cleared
Sep 26, 2006
NEX-LINK SPINAL FIXATION SYSTEM OFFSET CONNECTORS, 2121-XX SERIES
Orthopedic
29d
Cleared
Mar 31, 2006
NEX-LINK SPINAL FIXATION SYSTEM ROD TO ROD CONNECTORS, MODELS 725, 726 SERIES
Orthopedic
22d
Cleared
Mar 06, 2006
ABBOTT SPINE UNIVERSAL CLAMP SYSTEM
Orthopedic
62d
Cleared
Jan 06, 2006
NEX-LINK SPINAL FIXATION SYSTEM OPEN POLYAXIAL SCREWS, MODELS 2112, 2113,...
Orthopedic
109d
Cleared
Nov 07, 2005
ABBOTT SPINE, INC. SPINNAKER SYSTEM
Gastroenterology & Urology
42d
Cleared
Sep 14, 2005
NEX-LINK SPINAL FIXATION SYSTEM VARIABLE CROSSLINK, MODEL 721-XX
Orthopedic
27d