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VERIFLEX (LIBERTE) BARE-METAL CORONARY STENT SYSTEM

FDA premarket approval P040016 · decided 2005-04-12

Approval details

PMA number
P040016
Trade name
VERIFLEX (LIBERTE) BARE-METAL CORONARY STENT SYSTEM
Generic name
STENT, CORONARY
Applicant
Boston Scientific Scimed, Inc.
Date received
2004-03-26
Decision date
2005-04-12
Days to decision
382 days
Decision code
APWD
Product code
MAF
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
APPROVAL FOR THE BOSTON SCIENTIFIC CORPORATION LIBERTE MONORAIL AND OVER-THE-WIRE CORONARY STENT SYSTEMS. THE DEVICES ARE INDICATED FOR IMPROVING CORONARY LUMINAL DIAMETER IN PATIENTS WITH SYMPTOMATIC ISCHEMIC DISEASE WITH STENOTIC LESIONS IN NATIVE CORONARY ARTERIES (LENGTH <=28 MM) WITH A REFERENCE VESSEL DIAMETER OF 2.75 TO 5.00 MM.

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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