Cordis Neurovascular, Inc. - FDA 510(k) Cleared Devices
37
Total
37
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis Neurovascular, Inc. Neurology ✕
12 devices
Cleared
Sep 12, 2008
TRUFILL DCS SYRINGE
Neurology
29d
Cleared
May 02, 2008
TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE OR TRUFILL DCS...
Neurology
28d
Cleared
Sep 26, 2007
VASCULAR OCCLUSION SYSTEM (TRUFILL PUSHABLE COILS AND TRUPUSH COIL PUSHER)
Neurology
72d
Cleared
Dec 07, 2006
THE TRUFILL DCS DETACHABLE COIL SYSTEM
Neurology
41d
Cleared
Dec 15, 2005
TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM LINE EXTENSION
Neurology
29d
Cleared
Sep 23, 2003
TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE, ALSO KNOWN AS...
Neurology
35d
Cleared
Jun 20, 2003
TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE, ALSO KNOWN AS THE...
Neurology
85d
Cleared
Mar 24, 1999
VASCULAR OCCLUSION SYSTEM
Neurology
170d
Cleared
Jun 04, 1998
CES VASCULAR OCCLUSION SYSTEM
Neurology
303d
Cleared
Mar 21, 1997
TRUFILL PVA PARTICLES
Neurology
87d
Cleared
Jan 30, 1997
CES VASCULAR OCCLUSION SYSTEM
Neurology
90d
Cleared
Aug 08, 1995
TRUEFILL PVA PARTICLES
Neurology
138d