FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stent, Renal

PMA: P890017 · Supplement: S009 · Decision Jul 11, 2000
Classifications
1
FEI Numbers
16
Registration Numbers
16

Basic Information

Device Name
Stent, Renal
Trade Name
PALMAZ BALLOON EXPANDABLE STENT
PMA Number
P890017
Supplement Number
S009
Device Class
FDA Class 3
Product Code
NIN
Generic Name
STENT, RENAL
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
July 11, 2000
Date Received
May 26, 2000
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A REVISED INSTRUCTIONS FOR USE (IFU) FOR THE CORDIS PALMAZ(TM) BALLOON EXPANDABLE STENT.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NIN Stent, Renal