FDA 510(k) Application Details - K230623

Device Classification Name	Plate, Fixation, Bone   More FDA Info for this Device
510(K) Number	K230623
Device Name	Plate, Fixation, Bone
Applicant	Intrauma S.p.A Via Genova 19 Rivoli (TO) 10098 IT Other 510(k) Applications for this Company
Contact	Piero Costa Other 510(k) Applications for this Contact
Regulation Number	888.3030   More FDA Info for this Regulation Number
Classification Product Code	HRS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/06/2023
Decision Date	09/01/2023
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