Atlas FDA

MAXXUM PTCA CATHETER

FDA premarket approval P860019/S156 · decided 2000-02-01

Approval details

PMA number
P860019
Supplement
S156
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
MAXXUM PTCA CATHETER
Generic name
Catheters, transluminal coronary angioplasty, percutaneous
Applicant
Scimed Life Systems, Inc.
Date received
1999-08-03
Decision date
2000-02-01
Days to decision
182 days
Decision code
APPR
Product code
LOX
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
Additional approval for the MAXXUM PTCA Catheter (balloon diamters ranging from 2.5-4.0 mm), the post-delivery expansion of balloon expandable stents.

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510(k) clearances by this applicant

RecordFirmDate
SCIMED INFORMER PRESSURE WIRE SYSTEM (K974241)Scimed Life Systems, Inc.1998-11-12
SCIMED 6 FRENCH WISEGUIDE GUIDE CATHETER (K981788)Scimed Life Systems, Inc.1998-08-18
SCIMED QUEST FLOPPY AND MODERATE SUPPORT GUIDE WIRES (K980360)Scimed Life Systems, Inc.1998-04-29
SCIMED 6 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS (K974559)Scimed Life Systems, Inc.1998-02-23
SCIMED 7 FRENCH WISEGUIDE GUIDE CATHETER (K974684)Scimed Life Systems, Inc.1998-02-19
LUGE GUIDE WIRE (K973945)Scimed Life Systems, Inc.1998-01-12
SCIMED 8 FRENCH WISEGUIDE GUIDE CATHETER (K970823)Scimed Life Systems, Inc.1997-06-03
CHOICE SUPER SUPPORT PTCA GUIDE WIRE, CHOICE PLUS SUPER SUPPORT PTCA GUIDE WIRE, CHOICE EXCHANGE SUPER SUPPORT PTCA GUID (K964551)Scimed Life Systems, Inc.1997-05-21