Advanced Spine Fixation Systems, Inc. is one of 9745 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Spine Fixation Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: WILTSE SYSTEM, MODIFICATION TO PARTS NUMBERED CGT-SL AND CGT-SL-15, CENTRA-LINE GRAPPLE, VARIFIX SYSTEM
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.
FDA 510(k) Regulatory Record - Advanced Spine Fixation Systems, Inc.
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