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Precision Spectra, Precision Novi, Precision Montage, Precision Montage MRI an Spectra WaveWriter SPinal Cord Stimulator

FDA premarket approval P030017/S315 · decided 2018-08-01

Approval details

PMA number
P030017
Supplement
S315
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Precision Spectra, Precision Novi, Precision Montage, Precision Montage MRI an Spectra WaveWriter SPinal Cord Stimulator
Generic name
Stimulator, spinal-cord, totally implanted for pain relief
Applicant
Boston Scientific Corp
Date received
2018-07-02
Decision date
2018-08-01
Days to decision
30 days
Decision code
OK30
Product code
LGW
Advisory committee
Neurology
Expedited review
No
Location
Valencia, CA
Statement
Removal of the weekly Printed Circuit Board Assembly (PCBA) Ionic Contamination (IC) Testing on the Archie, Montana, and Spectra circuit boards which are used in the Implantable Pulse Generators (IPGs) for the Precision Spectra, Precision Novi, Precision Montage, Precision Montage MRI and Spectra WaveWriter Spinal Cord Stimulator (SCS) Systems.

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