FDA Product Code MCW: Catheter, Peripheral, Atherectomy
Peripheral artery disease caused by atherosclerotic plaque can be treated by directly removing the obstruction. FDA product code MCW covers peripheral atherectomy catheters.
These devices use rotating blades, laser energy, or orbital abrasion to debulk atherosclerotic plaque from peripheral arteries, restoring blood flow without the vessel stretching associated with balloon angioplasty. They are used in the treatment of femoral, popliteal, and tibial artery disease.
MCW devices are Class II medical devices, regulated under 21 CFR 870.4875 and reviewed by the FDA Cardiovascular panel.
Leading manufacturers include Eximo Medical, Ltd., Cardiovascular Systems, Inc. and Cardio Flow Inc.,.
146
Total
146
Cleared
102d
Avg days
1990
Since
146 devices
Cleared
Feb 06, 1998
THROMBOLYTIC BRUSH CATHETER, OVER THE WIRE (OTW)
Micro Therapeutics, Inc.
Cardiovascular
134d
Cleared
Aug 29, 1997
ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM WITH THE ROTALINK EXCHANGEABLE CATHETER
Boston Scientific Corp
Cardiovascular
214d
Cleared
Aug 08, 1997
THROMBOLYTIC BRUSH CATHETER
Micro Therapeutics, Inc.
Cardiovascular
312d
Cleared
Jul 25, 1997
ARROW-TREROTOLA PTD CATHETER
Arrow Intl., Inc.
Cardiovascular
197d
Cleared
Feb 19, 1992
TRAC-WRIGHT TRAC 10 CATHETER
Dow Corning Wright
Cardiovascular
90d
Cleared
Dec 27, 1990
THERATEK GROUP EXCHANGE CATHETER
Dow Corning Wright
Cardiovascular
73d