FDA 510(k) Application Details - K242340

Device Classification Name	Abutment, Implant, Dental, Endosseous   More FDA Info for this Device
510(K) Number	K242340
Device Name	Abutment, Implant, Dental, Endosseous
Applicant	Terrats Medical SL Carrer Mogoda 75-99 Barberα del VallΦs 08210 ES Other 510(k) Applications for this Company
Contact	Roger Terrats 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	08/07/2024
Decision Date	11/05/2024
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