FDA 510(k) Application Details - K210359

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Lumbar   More FDA Info for this Device
510(K) Number	K210359
Device Name	Intervertebral Fusion Device With Bone Graft, Lumbar
Applicant	SpineVision SAS 10 rue de la Renaissance Batiment E 92160 FR Other 510(k) Applications for this Company
Contact	Arnaud Brisard Other 510(k) Applications for this Contact
Regulation Number	888.3080   More FDA Info for this Regulation Number
Classification Product Code	MAX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/08/2021
Decision Date	03/10/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review