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EluNIR™ Ridaforolimus Eluting Coronary Stent System

FDA premarket approval P170008/S011 · decided 2019-02-13

Approval details

PMA number
P170008
Supplement
S011
Supplement type
135 Review Track For 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
2018-10-31
Decision date
2019-02-13
Days to decision
105 days
Decision code
APPR
Product code
NIQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Tel Aviv
Statement
Approval for introduction of a new analytical test method for determination of the concentration of the polymers in the drug solution, and removal of certain tests for the polymer stock solutions and the drug solution.

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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