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RADIUS CORONARY STENT WITH DELIVERY SYSTEM

FDA premarket approval P970061/S008 · decided 2000-02-11

Approval details

PMA number
P970061
Supplement
S008
Supplement type
Special (Immediate Track)
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
RADIUS CORONARY STENT WITH DELIVERY SYSTEM
Applicant
Boston Scientific Scimed, Inc.
Date received
2000-01-24
Decision date
2000-02-11
Days to decision
18 days
Decision code
APPR
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
Approval of the addition of two tensile strenght specifications for the pullwire assembly.

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510(k) clearances by this applicant

RecordFirmDate
MODIFICATION TO ATLANTIS PV IMAGING CATHETER, MODEL 36456 (K041727)Boston Scientific Scimed, Inc.2004-07-23
PT2 GUIDE WIRE AND ADDWIRE EXTENSION WIRE (K030617)Boston Scientific Scimed, Inc.2003-05-21
MODIFICATION TO BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM (K024048)Boston Scientific Scimed, Inc.2003-01-06
BOSTON SCIENTIFIC ULTRA-SOFT SV BALLOON DILATATION CATHETER (K021735)Boston Scientific Scimed, Inc.2002-08-08
WALLGRAFT TRACHEOBRONCHIAL ENDOPROTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM (K021901)Boston Scientific Scimed, Inc.2002-07-09
MODIFICIATION TO: BILIARY WALLSTENT ENDOPROSTHEIS WITH MONORAIL DELIVERY SYSTEM, MODEL 71-XXX (K012822)Boston Scientific Scimed, Inc.2001-10-24
NIROYAL BILIARY PREMOUNTED STENT SYSTEM (K012216)Boston Scientific Scimed, Inc.2001-08-17
BOSTON SCIENTIFIC SCIMED ATLANTIS CORONARY IMAGING CATHETER, MODEL C4020 (K000743)Boston Scientific Scimed, Inc.2000-09-06