Atlas FDA

Vercise Deep Brain Stimulation (DBS) Systems

FDA premarket approval P150031/S022 · decided 2019-09-04

Approval details

PMA number
P150031
Supplement
S022
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Vercise Deep Brain Stimulation (DBS) Systems
Generic name
Stimulator, electrical, implanted, for parkinsonian symptoms
Applicant
Boston Scientific Corp
Date received
2019-08-05
Decision date
2019-09-04
Days to decision
30 days
Decision code
APPR
Product code
NHL
Advisory committee
Neurology
Expedited review
No
Location
Valencia, CA
Statement
Approval of the Changes Being Effected (CBE) for the Vercise Deep Brain Stimulation (DBS) Systems. The changes being effected include changes to Vercise Deep Brain Stimulation (DBS) Systems physician and patient labeling, to enhance and harmonize the information regarding the risks of depression, suicide ideation, and suicide across the device type.

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