FDA 510(k) Application Details - K221021

Device Classification Name	Rod, Fixation, Intramedullary And Accessories   More FDA Info for this Device
510(K) Number	K221021
Device Name	Rod, Fixation, Intramedullary And Accessories
Applicant	Neoortho Produtos OrtopΘdicos S/A Rua ┬ngelo Domingos Durigan, 607 , Cascatinha Curitiba 82025-100 BR Other 510(k) Applications for this Company
Contact	Luciane Suzuki 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	04/06/2022
Decision Date	12/06/2022
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