FDA 510(k) Application Details - K230104

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K230104
Device Name	Implant, Endosseous, Root-Form
Applicant	Anthogyr 2237 Avenue AndrΘ Lasquin Sallanches 74700 FR Other 510(k) Applications for this Company
Contact	Estelle Salle 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	01/13/2023
Decision Date	10/16/2023
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