FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Electrical, Implanted, For Parkinsonian Symptoms

PMA: P150031 · Supplement: S085 · Decision May 29, 2025
Classifications
1
FEI Numbers
31
Registration Numbers
31

Basic Information

Device Name
Stimulator, Electrical, Implanted, For Parkinsonian Symptoms
Trade Name
VERCISE DEEP BRAIN STIMULATION (DBS)SYSTEM
PMA Number
P150031
Supplement Number
S085
Device Class
FDA Class 3
Product Code
NHL
Generic Name
Stimulator, electrical, implanted, for parkinsonian symptoms
Medical Specialty
Unknown
Advisory Committee
Neurology
Decision
Approved
Decision Code
APPR
Decision Date
May 29, 2025
Date Received
May 2, 2025
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for 1. Change to Item 6, Figure 21 to an image with a floating clip2. Added to Item 7, New Figure 22 with an extended lead (Figure 22. Push the Retaining Clip Into the Base)3. Added to Item 8: a. “Note: If you have difficulty locking the Slider, you may need to remove the Lead Stylet before locking the Slider in place, or replace the Retaining Clip using another Burr Hole Cover Kit or Burr Hole Cover Spares Kit.”b. Added New Figure 23 to include Lead and Screws (Figure 23. Lock the Slider) and remaining Figures shifted accordingly in sequence (previous Figure 23 is now Figure 24 etc.)4. Added to Item 9 Remove the Lead Stylet: “You may confirm the Slider is fully locked by repeating Step 8.”5. Changed Item 10 to “Verify that the DBS Lead has not moved from the desired location (e.g. by intraoperative imaging).” Previous Item 10 is now Item 11, and remaining steps shifted accordingly in sequence (previous Item 11 is now Item 12 etc) .

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NHL Stimulator, Electrical, Implanted, For Parkinsonian Symptoms