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DEEP BRAIN STIMULATION (DBS) LEAD CAP

FDA premarket approval P960009/S170 · decided 2013-06-03

Approval details

PMA number
P960009
Supplement
S170
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
DEEP BRAIN STIMULATION (DBS) LEAD CAP
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2013-03-21
Decision date
2013-06-03
Days to decision
74 days
Decision code
APPR
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
APPROVAL FOR THE IMPLEMENTATION OF MANUFACTURING PROCESS CHANGES, AND ADDITIONAL INSPECTIONAL STEPS, FOR THE DEVICE.

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