Atlas FDA

SCIMED PTCA CATHETER

FDA premarket approval P860019/S161 · decided 2000-04-26

Approval details

PMA number
P860019
Supplement
S161
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
SCIMED PTCA CATHETER
Generic name
Catheters, transluminal coronary angioplasty, percutaneous
Applicant
Scimed Life Systems, Inc.
Date received
2000-04-06
Decision date
2000-04-26
Days to decision
20 days
Decision code
OK30
Product code
LOX
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
Change in manufacturing method from an acid-etch to a centerless grinding process for the distal taper in the corewire subassembly in fixed wire models of PTCA catheters, including the Long ACE, Graft ACE, PIVOT, and ACE.

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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