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FDA 510(k) Application Details - K123373
Device Classification Name
Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
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510(K) Number
K123373
Device Name
Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
Applicant
LIFE SPINE
2401 Hassell Rd Ste 1535
Hoffman Est, IL 60169 US
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Contact
RANDY LEWIS
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Regulation Number
888.3070
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Classification Product Code
NKB
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More FDA Info for this Product Code
Date Received
11/01/2012
Decision Date
03/06/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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