The following data is part of a premarket notification filed by Medtronic, Inc. (formerly D.b.a. Ev3 Inc, Covidien Llc.) with the FDA for Evercrosstm 0.035 Otw Pta Dilatation Catheter.
| Device ID | K190753 |
| 510k Number | K190753 |
| Device Name: | EverCrossTM 0.035 OTW PTA Dilatation Catheter |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | Medtronic, Inc. (formerly D.b.a. Ev3 Inc, Covidien Llc.) 3033 Campus Drive, Suite N550 Plymouth, MN 55441 |
| Contact | Breanna Fautsch |
| Correspondent | Breanna Fautsch Medtronic, Inc. (formerly D.b.a. Ev3 Inc, Covidien Llc.) 3033 Campus Drive, Suite N550 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 | 2019-03-25 |
| Decision Date | 2019-04-23 |