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PTCA CATHETERS

FDA premarket approval P860019/S157 · decided 1999-11-03

Approval details

PMA number
P860019
Supplement
S157
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
PTCA CATHETERS
Generic name
Catheters, transluminal coronary angioplasty, percutaneous
Applicant
Scimed Life Systems, Inc.
Date received
1999-10-06
Decision date
1999-11-03
Days to decision
28 days
Decision code
OK30
Product code
LOX
Advisory committee
Cardiovascular
Expedited review
No
Location
Maple Grove, MN
Statement
The 30-Day Notice requested an alternate manufacturing method of attaching the proximal shaft to t he core wire sub-assembly on the following PTCA catheters: Viva(TM) P860019/S143; Maxxum(TM) P860019/S144; NC Maxxum(TM) P860019/S150; Adante(TM) P860019/S154.

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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