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MAGIC WALLSTENT ENDOPROSTHESIS

FDA premarket approval P980009/S006 · decided 2001-03-16

Approval details

PMA number
P980009
Supplement
S006
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
MAGIC WALLSTENT ENDOPROSTHESIS
Generic name
STENT, CORONARY
Applicant
Boston Scientific Scimed, Inc.
Date received
2001-02-23
Decision date
2001-03-16
Days to decision
21 days
Decision code
APPR
Product code
MAF
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
APPROVAL FOR A NEW MANUFACTURING SITE LOCATED AT BOSTON SCIENTIFIC IRELAND LTD., GALWAY, IRELAND.

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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