FDA Product Code PDU: Catheter For Crossing Total Occlusions
Chronic total occlusions present the most challenging lesions in interventional cardiology. FDA product code PDU covers catheters specifically designed to cross total coronary or peripheral occlusions.
These dedicated CTO catheters have stiff, tapered tips and hydrophilic coatings that facilitate penetration and crossing of completely occluded vessel segments, enabling guidewire delivery distal to the occlusion for subsequent revascularization.
PDU devices are Class II medical devices, regulated under 21 CFR 870.1250 and reviewed by the FDA Cardiovascular panel.
Leading manufacturers include Avinger, Inc., Spectranetics Corp. and Flowcardia, Inc..
58
Total
58
Cleared
106d
Avg days
2003
Since
58 devices
Cleared
Mar 30, 2006
RF TUNNELER WIRE
Baylis Medical Co., Inc.
Cardiovascular
281d
Cleared
Oct 19, 2005
CLIRPATH TURBO PLUS EXCIMER LASER CATHETERS, MODELS 314-151, 314-159, 317-152, 317-156, 320-006, 320-159, 323-001
Spectranetics Corp.
Cardiovascular
35d
Cleared
Sep 02, 2005
CLIRPATH TURBO EXCIMER LASER CATHETERS
Spectranetics Corp.
Cardiovascular
10d
Cleared
Aug 18, 2005
2.5 MM TURBO CLIRPATH EXCIMER LASER CATHETER, MODEL 225-011
Spectranetics Corp.
Cardiovascular
246d
Cleared
Jun 08, 2005
SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM [PERIPHERAL]
Intra Luminal Therapeutics, Inc.
Cardiovascular
57d
Cleared
Apr 27, 2004
CLIRPATH EXCIMER LASER CATHETER
Spectranetics Corp.
Cardiovascular
104d
Cleared
Jan 07, 2004
LUMEND FRONTRUNNER CTO CATHETER AND ACCESSORIES
Lumend, Inc.
Cardiovascular
58d
Cleared
Nov 21, 2003
SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM
Intra Luminal Therapeutics, Inc.
Cardiovascular
158d
Cleared
Jun 18, 2003
LUMEND FRONTRUNNER GW CTO CATHETER
Lumend, Inc.
Cardiovascular
79d
Cleared
Jan 23, 2003
LUMEND FRONTRUNNER CTO CATHETER
Lumend, Inc.
Cardiovascular
126d