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510(k) K982902

PERIPHERAL NERVE STIMULATION by Medtronic Vascular — Product Code GZF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 10, 1998
Date Received
August 14, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stimulator, Peripheral Nerve, Implanted (Pain Relief)
Device Class
Class II
Regulation Number
882.5870
Review Panel
NE
Submission Type

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