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EluNIR™ Ridaforolimus Eluting Coronary Stent System

FDA premarket approval P170008/S044 · decided 2023-05-09

Approval details

PMA number
P170008
Supplement
S044
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
EluNIR™ Ridaforolimus Eluting Coronary Stent System
Generic name
Coronary drug-eluting stent
Applicant
Medinol, Ltd.
Date received
2023-04-27
Decision date
2023-05-09
Days to decision
12 days
Decision code
OK30
Product code
NIQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Tel Aviv
Statement
Replacing the vacuum oven used as part of EluNIR's delivery system manufacturing process of assembling markers on the distal inner shaft tube.

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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