Micro Therapeutics, Inc. - FDA 510(k) Cleared Devices
51
Total
50
Cleared
0
Denied
FDA 510(k) Regulatory Record - Micro Therapeutics, Inc. Neurology ✕
11 devices
Cleared
Apr 24, 2007
FX DETACHABLE COIL SYSTEM
Neurology
400d
Cleared
Apr 20, 2006
NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR
Neurology
42d
Cleared
Jun 28, 2005
NEXUS DETACHABLE COIL, MULTI-DIAMETER CSR AND HELIX SUPER SOFT CSR
Neurology
15d
Cleared
Jun 22, 2005
NEXUS DETACHABLE COIL SYSTEM, HELIX SUPER SOFT CSR
Neurology
21d
Cleared
Apr 27, 2005
NEXUS DETACHABLE COIL SYSTEM
Neurology
56d
Cleared
Jul 16, 2004
SAPPHIRE NXT DETACHABLE COIL SYSTEM
Neurology
29d
Cleared
Mar 25, 2004
MODIFICATION TO SAPPHIRE DETACHABLE COIL SYSTEM (TETRIS 3-D)
Neurology
8d
Cleared
Jan 09, 2004
SAPPHIRE DETACHABLE FIBERED COIL SYSTEM, HELIX FIBERED, CYCLONE, MULTIPLE MODELS
Neurology
79d
Cleared
Sep 25, 2003
SAPPHIRE VDS TENSION SAFE DETACHABLE COIL, E-3-12/3-T10-VT
Neurology
43d
Cleared
Aug 20, 2003
SAPPHIRE DETACHABLE FIBER COILS
Neurology
65d
Cleared
Jul 21, 2003
SAPPHIRE DETACHABLE COIL SYSTEM
Neurology
166d