The following data is part of a premarket notification filed by Ev3 Inc with the FDA for Evercross 0.035 Otw Pta Dilation Catheter.
| Device ID | K103322 |
| 510k Number | K103322 |
| Device Name: | EVERCROSS 0.035 OTW PTA DILATION CATHETER |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | EV3 INC 3033 Campus Drive Plymouth, MN 55441 |
| Contact | David Worrell, Ms, Rac |
| Product Code | LIT |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2010-11-12 |
| Decision Date | 2010-12-06 |