FDA 510(k) Application Details - K222738

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K222738
Device Name	Implant, Endosseous, Root-Form
Applicant	PointNix Co., Ltd B1 and 3F, 7, Hyoyeol-ro Buk-gu 46509 KR Other 510(k) Applications for this Company
Contact	Chang Nam Lee 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	09/09/2022
Decision Date	04/13/2023
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