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PARAGON, PHOENIX, MULTILOG & SENSORITHM PACEMAKERS

FDA premarket approval P830045/S101 · decided 2006-08-09

Approval details

PMA number
P830045
Supplement
S101
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
PARAGON, PHOENIX, MULTILOG & SENSORITHM PACEMAKERS
Generic name
Pulse generator, permanent, implantable
Applicant
St. Jude Medical, Inc.
Date received
2006-07-13
Decision date
2006-08-09
Days to decision
27 days
Decision code
OK30
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
CHANGE TO AN AUTOMATED SELECTIVE SOLDERING PROCESS AS AN ALTERNATE METHOD FOR THE SOLDERING ON THE PEPIN BOARD OF THE MODEL 3650 MERLIN PCS.

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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