FDA 510(k) Application Details - K200312

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Cervical   More FDA Info for this Device
510(K) Number	K200312
Device Name	Intervertebral Fusion Device With Bone Graft, Cervical
Applicant	Spineart 3 Chemin du pre Fleuri Plan Les Ouates 1228 CH Other 510(k) Applications for this Company
Contact	Frank Pennesi Other 510(k) Applications for this Contact
Regulation Number	888.3080   More FDA Info for this Regulation Number
Classification Product Code	ODP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/06/2020
Decision Date	04/06/2020
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