Boston Scientific Precision - Page 4

Precision™ Spinal Cord Stimulator System Clinician Manual
Clinician Manual
97035873-01 iv of iv
Securing the Innion CX Trial Lead ........................................................................................... 32
Permanent Lead Anchoring and Tunneling ...............................................................................33
Anchoring the Lead ........................................................................................................................34
Tunneling the Lead or Lead Extension ..........................................................................................35
Connecting the Lead Extension ..................................................................................................... 37
Connecting to the Trial Stimulator .............................................................................................39
Removal of Trial Leads, Extensions, and Splitters ...................................................................41
Option A: Percutaneous Lead Removal after Temporary Trial .......................................................41
Option B: Lead Extension Removal after Permanent Trial ............................................................41
Option C: Splitter Removal after Trial .............................................................................................41
IPG Implantation .......................................................................................................................... 42
Connecting to the IPG .................................................................................................................43
For Percutaneous Lead - Dual Lead Connection ..........................................................................43
For Innion™ 16 Lead Connection .................................................................................................43
For Innion CX Lead Connection ....................................................................................................43
For Percutaneous Lead - Single Lead Connection ........................................................................ 43
For Surgical Paddle Lead Connection ...........................................................................................43
Programming with the Innion 16 Lead and Innion CX Lead ........................................................45
IPG Explant or Replacement ......................................................................................................46
Rechargeable Stimulator System ..............................................................................................47
IPG Battery Status .........................................................................................................................47
Charging Steps ..............................................................................................................................48
Patient Remote Control ..................................................................................................................50
Device Linking ...............................................................................................................................54
Searching .......................................................................................................................................55
Clinician Options ............................................................................................................................. 55
Remote Control Battery Life ...........................................................................................................60
Specications and Technical Data .............................................................................................61
Materials ........................................................................................................................................61
Max Current Amp. per Electrode vs. Impedance ...........................................................................62
Registration Information ..............................................................................................................65
Registering the Stimulator and Leads ............................................................................................65
Technical Service ........................................................................................................................66
Electromagnetic Compatibility ....................................................................................................67
EN 60601-1-2 Classication Information ........................................................................................67
Limited Warranty - IPG ................................................................................................................ 72
Limited Warranty - Leads ............................................................................................................ 73
Limited Warranty - Externals ....................................................................................................... 74
Patient Identication ...................................................................................................................75