The following data is part of a premarket notification filed by Ev3 Inc with the FDA for Nanocross Eite 0.014 Over-the-wire Pta Balloon Dilatation Catheter.
Device ID | K141118 |
510k Number | K141118 |
Device Name: | NANOCROSS EITE 0.014 OVER-THE-WIRE PTA BALLOON DILATATION CATHETER |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | EV3 INC 3033 Campus Drive Suite N550 Plymouth, MN 55441 |
Contact | Laura J Lind |
Correspondent | Laura J Lind EV3 INC 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 | 2014-04-30 |
Decision Date | 2014-07-18 |
Summary: | summary |