The following data is part of a premarket notification filed by Ev3 Inc. with the FDA for Rapidcross Pta Rapid Exchange Balloon Dilatation Catheter.
Device ID | K130911 |
510k Number | K130911 |
Device Name: | RAPIDCROSS PTA RAPID EXCHANGE BALLOON DILATATION CATHETER |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | EV3 INC. 3033 Campus Drive Plymouth, MN 55441 |
Contact | Laura J Lind |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | LIT |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2013-04-02 |
Decision Date | 2013-05-24 |
Summary: | summary |