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 |