FDA 510(k) Application Details - K230817

Device Classification Name	More FDA Info for this Device
510(K) Number	K230817
Device Name	TORPEDO Implant System«
Applicant	Deltacor GmbH Rudolf-Diesel-Str. 10 Werneck D-97440 DE Other 510(k) Applications for this Company
Contact	Maximilian Reuss Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OUR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/24/2023
Decision Date	01/19/2024
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