FDA 510(k) Application Details - K203399

Device Classification Name	Rod, Fixation, Intramedullary And Accessories   More FDA Info for this Device
510(K) Number	K203399
Device Name	Rod, Fixation, Intramedullary And Accessories
Applicant	WITTENSTEIN intens GmbH Walter-Wittensstein-StraBe 1 Igersheim 97999 DE Other 510(k) Applications for this Company
Contact	Hartmut Kampa Other 510(k) Applications for this Contact
Regulation Number	888.3020   More FDA Info for this Regulation Number
Classification Product Code	HSB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/19/2020
Decision Date	02/17/2021
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