Advanced Spine Fixation Systems, Inc. - FDA 510(k) Cleared Devices
16
Total
7
Cleared
0
Denied
Advanced Spine Fixation Systems, Inc. has 7 FDA 510(k) cleared orthopedic devices. Based in Washington, US.
Historical record: 7 cleared submissions from 1989 to 2000.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
16 devices
Cleared
Feb 04, 2000
WILTSE SYSTEM
Orthopedic
234d
Cleared
Apr 13, 1999
MODIFICATION TO PARTS NUMBERED CGT-SL AND CGT-SL-15
Orthopedic
29d
Cleared
Jan 25, 1996
CENTRA-LINE GRAPPLE, VARIFIX SYSTEM
Orthopedic
100d
Cleared
Nov 07, 1995
SADDLE WITH ANCHOR, STAINLESS STEEL VARIFIX SYSTEM
Orthopedic
85d
Cleared
Nov 06, 1995
SADDLE WITH ANCHOR, TITANIUM VARIFIX SYSTEM
Orthopedic
84d
Cleared
Sep 08, 1995
STAINLESS STEEL VARIFIX SYSTEM 5.0MM DIAMETER ANCHOR SCREW
Orthopedic
52d
Cleared
Jul 26, 1995
5.8MM DIAMETER ANCHOR SCREW
Orthopedic
126d
Cleared
Jul 25, 1995
TITANIUM LOW PROFILE CROSS BAR
Orthopedic
132d
Cleared
Apr 26, 1995
SELBY INSTRUMENTATION
Orthopedic
267d
Cleared
Apr 26, 1995
SELBY INSTRUMENTATION
Orthopedic
194d
Cleared
Feb 14, 1995
SELBY INSTRUMENTATION
Orthopedic
271d
Cleared
May 02, 1994
LOW PROFILE MID CROSS BRACING
Orthopedic
418d
Cleared
Mar 28, 1994
LOW PROFILE SLEAVE NUT ASSEMBLY
Orthopedic
383d
Cleared
Sep 21, 1993
SELBY INSTRUMENTATION
Orthopedic
383d
Cleared
May 05, 1992
THE SELBY SYSTEM
Orthopedic
117d
Cleared
Jun 22, 1989
SELBY INSTRUMENTATION
Orthopedic
202d