The following data is part of a premarket notification filed by Ev3 Inc with the FDA for Powercross .018 Otw Pta Dilation Catheter.
Device ID | K093286 |
510k Number | K093286 |
Device Name: | POWERCROSS .018 OTW PTA DILATION CATHETER |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | EV3 INC 3033 Campus Drive Plymouth, MN 55441 |
Contact | Sara Bakker |
Correspondent | Sara Bakker EV3 INC 3033 Campus Drive Plymouth, MN 55441 |
Product Code | LIT |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-10-20 |
Decision Date | 2009-11-13 |
Summary: | summary |