Atlas FDA

CADENCE TIERED-THERAPY DEFIBRILLATOR SYSTEM

FDA premarket approval P910023/S171 · decided 2008-04-11

Approval details

PMA number
P910023
Supplement
S171
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CADENCE TIERED-THERAPY DEFIBRILLATOR SYSTEM
Generic name
Pulse generator, permanent, implantable
Applicant
ABBOTT MEDICAL
Date received
2008-03-25
Decision date
2008-04-11
Days to decision
17 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
APPROVAL FOR ENHANCEMENTS TO THE SOFTWARE (VERSION 3.0) USED IN THE ST. JUDE MEDICAL MERLIN.NET SYSTEM.

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