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PHOENIX 2 AND PARAGON II PACING SYSTEMS

FDA premarket approval P830045/S051 · decided 1996-10-09

Approval details

PMA number
P830045
Supplement
S051
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
PHOENIX 2 AND PARAGON II PACING SYSTEMS
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
St. Jude Medical, Inc.
Date received
1996-03-12
Decision date
1996-10-09
Days to decision
211 days
Decision code
APPR
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
MODIFICATION OF LABELING TO INCLUDE A "CELLULAR TESTED" LOGO TO THE SHELF PACKAGE OF THE FOLLOWING PACEMAKER MODELS: PHOENIX 2 (2005/2008/2009), PARAGON (2010/2011/2012), PARAGON II (2016), SYNCHRONY (2020), SYNCHRONY II (2022/2023), SYNCHRONY III (2028/2029), SOLUS (2002/2003), SOLUS II (2006/2007), TRILOGY (2350/2308/2250) AND REVISION OF THE PATIENT MANUAL TO INCLUDE THE LOGO AND LANGUAGE INFORMING THE PATIENT THAT NO SPECIAL CELL PHONE PRECAUSTIONS NEED BE TAKEN BY PATIENTS RECEIVING THESE M

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510(k) clearances by this applicant

RecordFirmDate
Advisor HD Grid Mapping Catheter, Sensor Enabled (K172393)St. Jude Medical, Inc.2018-04-23
Confirm Rx Insertable Cardiac Monitor (ICM) System (K163407)St. Jude Medical, Inc.2017-09-29
PressureWire X Guidewire (K161171)St. Jude Medical, Inc.2016-08-15
Nanostim Introducer Kit (K161102)St. Jude Medical, Inc.2016-05-19
The Nanostim Introducer Kit (K160716)St. Jude Medical, Inc.2016-04-14
NANOSTIM INTRODUCER KIT (K140793)St. Jude Medical, Inc.2014-12-17
SJM CONFIRM IMPLANTABLE CARDIAC MONITOR (ICM) (K133481)St. Jude Medical, Inc.2014-05-28
ENLIGHTN RENAL GUIDE CATHETER (K131592)St. Jude Medical, Inc.2014-01-31