510(k) K093286

POWERCROSS .018 OTW PTA DILATION CATHETER by Ev3, Inc. — Product Code LIT

K093286 is an FDA 510(k) premarket notification submitted by Ev3, Inc. for the device "POWERCROSS .018 OTW PTA DILATION CATHETER". The FDA issued a decision of Substantially Equivalent on November 13, 2009. The device falls under product code LIT (Catheter, Angioplasty, Peripheral, Transluminal), a Class II device regulated under 21 CFR 870.1250. Ev3, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 13, 2009
Date Received
October 20, 2009
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Angioplasty, Peripheral, Transluminal
Device Class
Class II
Regulation Number
870.1250
Review Panel
CV
Submission Type