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FDA 510(k) Application Details - K170650
Device Classification Name
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
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510(K) Number
K170650
Device Name
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Applicant
Orthofix Srl
Via Delle Nazioni 9
Bussolengo 37012 IT
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Contact
Gianluca Ricadona
Other 510(k) Applications for this Contact
Regulation Number
888.3030
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Classification Product Code
KTT
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More FDA Info for this Product Code
Date Received
03/03/2017
Decision Date
05/10/2017
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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