Atlas FDA

8085 PREVAIL IMPLANTABLE PULSE GENERATOR

FDA premarket approval P850051/S055 · decided 2000-07-21

Approval details

PMA number
P850051
Supplement
S055
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
8085 PREVAIL IMPLANTABLE PULSE GENERATOR
Generic name
Pulse-generator, single chamber, sensor driven, implantable
Applicant
Medtronic, Inc.
Date received
2000-06-30
Decision date
2000-07-21
Days to decision
21 days
Decision code
APPR
Product code
LWO
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
APPROVAL FOR THE USE OF HEADER PART NUMBER 149422-002 IN THE FOLLOWING PULSE GENERATORS: PREVAIL MODEL 8085, PREVA SR MODEL 8089, PRODIGY S MODEL 8165, PRODIGY SR MODEL 8161, THERA-I S MODEL 8965I, THERA-I SR MODEL 8961I, VITATRON VISA S MODEL 115 AND VITATRON VISA SR MODEL 415.

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