Atlas FDA

VERITY ADX XL VDR MODEL 5456I PULSE GENERATOR

FDA premarket approval P830045/S090 · decided 2004-01-30

Approval details

PMA number
P830045
Supplement
S090
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
VERITY ADX XL VDR MODEL 5456I PULSE GENERATOR
Generic name
Programmer, pacemaker
Applicant
St. Jude Medical, Inc.
Date received
2003-12-02
Decision date
2004-01-30
Days to decision
59 days
Decision code
APPR
Product code
KRG
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
APPROVAL TO MODIFY THE HEADER DESIGN OF A CURRENTLY MARKETED DEVICE. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME VERITY ADX XL VDR MODEL 5456I AND IS INDICATED AS FOLLOWS: THE VERITY ADX XL VDR MODEL 5456I IS INDICATED FOR USE ONLY WITH AV PLUS MODEL 1328C OR 1358C SINGLE-PASS IN-LINE QUADRIPOLAR LEADS (THE VERITY ADX XL VDR PACING SYSTEM). THE VERITY ADX XL VDR PACING SYSTEM IS INTENDED TO PROVIDE VDD OR VDDR PACING FOR PATIENTS WITH A HEALTHY SINUS NODE AND AV CONDUCTION ABN

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