FDA 510(k) Application Details - K212702

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K212702
Device Name	Implant, Endosseous, Root-Form
Applicant	Guilin FiTeeth Medical Instrument Co., Ltd. Southeast Side of Renmin Road Extension Line, Yangtang Industrial Park, Lingui District Guilin 541199 CN Other 510(k) Applications for this Company
Contact	Jun Zhou Other 510(k) Applications for this Contact
Regulation Number	872.3640   More FDA Info for this Regulation Number
Classification Product Code	DZE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/26/2021
Decision Date	10/13/2022
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