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FDA 510(k) Application Details - K031833
Device Classification Name
Orthosis, Spinal Pedicle Fixation
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510(K) Number
K031833
Device Name
Orthosis, Spinal Pedicle Fixation
Applicant
MEDTRONIC SOFAMOR DANEK
1800 PYRAMID PLACE
MEMPHIS, TN 38132 US
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Contact
RICHARD TREHARNE
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Regulation Number
888.3070
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Classification Product Code
MNI
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More FDA Info for this Product Code
Date Received
06/13/2003
Decision Date
09/03/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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