Atlas FDA

EXPRESS2 CORONARY STENT SYSTEM

FDA premarket approval P020009/S068 · decided 2011-01-13

Approval details

PMA number
P020009
Supplement
S068
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
EXPRESS2 CORONARY STENT SYSTEM
Generic name
STENT, CORONARY
Applicant
Boston Scientific Scimed, Inc.
Date received
2010-12-14
Decision date
2011-01-13
Days to decision
30 days
Decision code
OK30
Product code
MAF
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
CHANGE IN THE ENVIRONMENTAL QUALITY CONTROL PROCEDURE.

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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