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510(k) K130545

MULTI LEAD TRIAL CABLE by St Jude Medical — Product Code GZB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 18, 2013
Date Received
March 1, 2013
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stimulator, Spinal-Cord, Implanted (Pain Relief)
Device Class
Class II
Regulation Number
882.5880
Review Panel
NE
Submission Type

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