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 |