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FDA 510(k) Application Details - K200148
Device Classification Name
Bracket, Ceramic, Orthodontic
More FDA Info for this Device
510(K) Number
K200148
Device Name
Bracket, Ceramic, Orthodontic
Applicant
LightForce Orthodontics
1035 Cambridge Street, Suite 14a
Cambridge, MA 02141 US
Other 510(k) Applications for this Company
Contact
Amos N Benninga
Other 510(k) Applications for this Contact
Regulation Number
872.5470
More FDA Info for this Regulation Number
Classification Product Code
NJM
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/22/2020
Decision Date
02/21/2020
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
Y
Expedited Review
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