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FDA 510(k) Application Details - K080502
Device Classification Name
Orthosis, Spinal Pedicle Fixation
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510(K) Number
K080502
Device Name
Orthosis, Spinal Pedicle Fixation
Applicant
LIFE SPINE
2401 W. HASSELL RD.
SUITE 1535
HOFFMAN ESTATES, IL 60169 US
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Contact
REBECCA M BROOKS
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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
02/25/2008
Decision Date
04/08/2008
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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