FDA PMA FDA Class 3 Approved 🇺🇸 United States

Pump, Infusion, Implanted, Programmable

PMA: P890055 · Supplement: S003 · Decision Sep 22, 1997
Classifications
1
FEI Numbers
18
Registration Numbers
18

Basic Information

Device Name
Pump, Infusion, Implanted, Programmable
Trade Name
CONSTANT FLOW IMPLANTABLE PUMP WITH BOLUS SAFETY VALVE
PMA Number
P890055
Supplement Number
S003
Device Class
FDA Class 3
Product Code
LKK
Generic Name
Pump, infusion, implanted, programmable
Medical Specialty
Unknown
Advisory Committee
General Hospital
Decision
Approved
Decision Code
APPR
Decision Date
September 22, 1997
Date Received
February 26, 1997
Supplement Type
Normal 180 Day Track
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for the intraspinal delivery of preservative free morphine for patient with intractable chronic pain.

Classifications

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

Product Code Device Name
LKK Pump, Infusion, Implanted, Programmable