FDA 510(k) Application Details - K240699

Device Classification Name	More FDA Info for this Device
510(K) Number	K240699
Device Name	SCARLET« AC-Ti
Applicant	Spineart SA Chemin du PrΘ-Fleuri 3 Plan-les-Ouates 1228 CH Other 510(k) Applications for this Company
Contact	Estelle Lefeuvre Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OVE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/14/2024
Decision Date	05/10/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review