FDA 510(k) Application Details - K231559

Device Classification Name	Abutment, Implant, Dental, Endosseous   More FDA Info for this Device
510(K) Number	K231559
Device Name	Abutment, Implant, Dental, Endosseous
Applicant	Talladium Espa±a, SL Virginia Woolf, 17 Lleida 25005 ES Other 510(k) Applications for this Company
Contact	Xavier Soca Filella 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	05/30/2023
Decision Date	11/17/2023
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