Atlas FDA

EluNIR™ Ridaforolimus Eluting Coronary Stent System

FDA premarket approval P170008 · decided 2017-11-28

Approval details

PMA number
P170008
Trade name
EluNIR™ Ridaforolimus Eluting Coronary Stent System
Generic name
Coronary drug-eluting stent
Applicant
Medinol, Ltd.
Date received
2017-03-13
Decision date
2017-11-28
Days to decision
260 days
Decision code
APPR
Product code
NIQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Tel Aviv
Statement
Approval for the EluNIR Ridaforolimus Eluting Coronary Stent System. This device is indicated for improving coronary luminal diameter in patients with symptomatic heart disease due to de novo lesions <=30mm in length in native coronary arteries with reference diameter of 2.50mm to 4.25mm.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
Gallant PTCA Dilatation Catheter (K173581)Medinol, Ltd.2018-01-25
NC Gallant PTCA Catheter (K162434)Medinol, Ltd.2017-01-19
X-Suit NIR Biliary Metallic Stent (K150487)Medinol, Ltd.2016-02-12
MEDINOL X-SUIT NIR BILIARY METALLIC STENT (K081956)Medinol, Ltd.2009-01-09
NIR BILIARY STENT (K002130)Medinol, Ltd.2000-10-30
NIR BILIARY STENT (K973171)Medinol, Ltd.1998-11-13