FDA 510(k) Application Details - K232733

Device Classification Name	Cerclage, Fixation   More FDA Info for this Device
510(K) Number	K232733
Device Name	Cerclage, Fixation
Applicant	Medacta International S.A. Strada Regina Castel San Pietro 6874 CH Other 510(k) Applications for this Company
Contact	Stefano Baj Other 510(k) Applications for this Contact
Regulation Number	888.3010   More FDA Info for this Regulation Number
Classification Product Code	JDQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/07/2023
Decision Date	05/03/2024
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