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 |