FDA 510(k) Application Details - K242072

Device Classification Name	Implant, Endosseous, Root-Form   More FDA Info for this Device
510(K) Number	K242072
Device Name	Implant, Endosseous, Root-Form
Applicant	CeraRoot SL Parpers 13 Les Franqueses del Valles 08520 ES Other 510(k) Applications for this Company
Contact	Josep Oliva-Ochoa 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	07/16/2024
Decision Date	05/14/2025
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