PMA supplement

P150031 S039: Vercise, Vercise PC, Vercise Gevia, Vercise Genus Deep Brain Stimulation Systems

FDA PMA supplement · 135 Review Track For 30-Day Notice · Boston Scientific Corp

Key facts

Original PMA P150031
Supplement number S039
Supplement type 135 Review Track For 30-Day Notice
Reason for the supplement Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name Vercise, Vercise PC, Vercise Gevia, Vercise Genus Deep Brain Stimulation Systems
Generic name Stimulator, electrical, implanted, for parkinsonian symptoms
Applicant Boston Scientific Corp
Product code NHL
Received date Jan 29, 2021
Decision date Nov 15, 2021

At a glance

  • No Expedited review granted
  • No Approval order on file
  • No Summary of safety and effectiveness on file

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About PMA supplements

A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.

Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date:

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