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FDA 510(k) Application Details - K162609
Device Classification Name
Aligner, Sequential
More FDA Info for this Device
510(K) Number
K162609
Device Name
Aligner, Sequential
Applicant
ClearPath Orthodontics Ltd
6-N, Main Boulevard
Johar Town PK
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Contact
Waqas Wahab
Other 510(k) Applications for this Contact
Regulation Number
872.5470
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Classification Product Code
NXC
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More FDA Info for this Product Code
Date Received
09/19/2016
Decision Date
07/06/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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