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FDA 510(k) Application Details - K201323
Device Classification Name
Abutment, Implant, Dental, Endosseous
More FDA Info for this Device
510(K) Number
K201323
Device Name
Abutment, Implant, Dental, Endosseous
Applicant
Cowellmedi Co., Ltd.
48, Hakgam-daero 221beon-gil, Sasang-gu
Busan 46986 KR
Other 510(k) Applications for this Company
Contact
Minjin Park
Other 510(k) Applications for this Contact
Regulation Number
872.3630
More FDA Info for this Regulation Number
Classification Product Code
NHA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/18/2020
Decision Date
01/25/2022
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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