Atlas FDA

RAPTORRAIL RX SDS, 2.25MM CYPHER STENT

FDA premarket approval P020026/S017 · decided 2009-09-18

Approval details

PMA number
P020026
Supplement
S017
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
RAPTORRAIL RX SDS, 2.25MM CYPHER STENT
Generic name
Coronary drug-eluting stent
Applicant
Cordis Corp.
Date received
2006-04-03
Decision date
2009-09-18
Days to decision
1264 days
Decision code
APPR
Product code
NIQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Fremont, CA
Statement
APPROVAL FOR THE 2.25 MM CYPHER STENT ON RAPTORRAIL RX STENT DELIVERY SYSTEM. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME CYPHER AND IS INDICATED FOR IMPROVING CORONARY LUMINAL DIAMETER IN PATIENTS WITH SYMPTOMATIC ISCHEMIC DISEASE DUE TO DISCRETE DE NOVO LESIONS OF LENGTH <= 30 MM IN NATIVE CORONARY ARTERIES WITH A REFERENCE VESSEL DIAMETER OF >=2.25 TO <=3.50 MM.

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
FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM; S.M.A.R.T. RE-FLEX BILIARY ELF-EXPANDING STENT SYSTEM (K130981)Cordis Corp.2014-03-12
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER (K112797)Cordis Corp.2012-05-04
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE (K101651)Cordis Corp.2010-07-09
MICRO GUIDE CATHETER XP (K082143)Cordis Corp.2008-08-25
SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MB (K062798)Cordis Corp.2008-02-06
PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAX (K060877)Cordis Corp.2006-04-27
CORDIS AMIIA .014 PTA BALLOON CATHETER (K050645)Cordis Corp.2005-04-01
CORDIS STEER-IT DEFLECTING TIP GUIDEWIRE (K040592)Cordis Corp.2004-12-17