FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stent, Coronary

PMA: P970061 · Supplement: S004 · Decision Sep 25, 1998
Classifications
1
FEI Numbers
28
Registration Numbers
28

Basic Information

Device Name
Stent, Coronary
Trade Name
SCIMED RADIUS CORONARY STENT WITH DELIVERY SYSTEM
PMA Number
P970061
Supplement Number
S004
Device Class
FDA Class 3
Product Code
MAF
Generic Name
STENT, CORONARY
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
September 25, 1998
Date Received
September 4, 1998
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for revisions to the Instructions for Use.

Classifications

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

Product Code Device Name
MAF Stent, Coronary