Atlas FDA

THOR PTCA DILATATION CATHETERS WITH 10 MM AND 40 MM LONG BALLOONS

FDA premarket approval P880003/S066 · decided 1997-04-30

Approval details

PMA number
P880003
Supplement
S066
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
THOR PTCA DILATATION CATHETERS WITH 10 MM AND 40 MM LONG BALLOONS
Generic name
Catheters, transluminal coronary angioplasty, percutaneous
Applicant
Cordis Corp.
Date received
1996-12-11
Decision date
1997-04-30
Days to decision
140 days
Decision code
APPR
Product code
LOX
Advisory committee
Cardiovascular
Expedited review
No
Location
Miami Lakes, FL
Statement
APPROVAL FOR THOR(TM) PTCA DILATATION CATHETERS WITH 10 MM AND 40 MM LONG BALLOONS

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