St. Jude Medical Neuromodulation is one of 5297 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
St. Jude Medical Neuromodulation - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
St. Jude Medical Neuromodulation has 2 FDA 510(k) cleared medical devices. Based in Plano, US.
Historical record: 2 cleared submissions from 2011 to 2013. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by St. Jude Medical Neuromodulation Filter by specialty or product code using the sidebar.
St. Jude Medical Neuromodulation — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jan 18, 2013
MTS SYSTEM, WIDE-SPACE QUATTRODE PERCUTANEOUS LEADS
Neurology
87d
Cleared
Nov 17, 2011
OCTRODEX(TM), QUATTRODEX(TM), INTRODEX(TM), EPIDURAL NEEDLE, STYLETS
Neurology
107d