Atlas FDA

Activa Deep Brain Stimulation Therapy System

FDA premarket approval P960009/S336 · decided 2019-03-01

Approval details

PMA number
P960009
Supplement
S336
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Activa Deep Brain Stimulation Therapy System
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2018-12-18
Decision date
2019-03-01
Days to decision
73 days
Decision code
APPR
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
Approval to add a Polyethylene terephthalate (PET) slip tube over proximal end of each cable conductor to prevent mechanical locking of the build epoxy to the Ethylene tetrafluoroethylene (ETFE) coated wire cables for DBS Extension models 37085 and 37086.

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