Atlas FDA

Activa Deep Brian Stimulation Therapy System

FDA premarket approval P960009/S335 · decided 2019-01-08

Approval details

PMA number
P960009
Supplement
S335
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Activa Deep Brian Stimulation Therapy System
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2018-12-11
Decision date
2019-01-08
Days to decision
28 days
Decision code
OK30
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
Manufacturing transfer of the M926634A001 Crimp Sleeve, from the current supplier Lake Region Medical to RMS.

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