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FDA 510(k) Application Details - K955291
Device Classification Name
Stimulator, Spinal-Cord, Implanted (Pain Relief)
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510(K) Number
K955291
Device Name
Stimulator, Spinal-Cord, Implanted (Pain Relief)
Applicant
MEDTRONIC VASCULAR
800 53RD AVE., N.E.
MINNEAPOLIS, MN 55421 US
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Contact
DENNIS H CRANE
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Regulation Number
882.5880
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Classification Product Code
GZB
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More FDA Info for this Product Code
Date Received
11/16/1995
Decision Date
05/17/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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