FDA 510(k) Application Details - K200235

Device Classification Name	Spinal Vertebral Body Replacement Device   More FDA Info for this Device
510(K) Number	K200235
Device Name	Spinal Vertebral Body Replacement Device
Applicant	icotec ag Industriestrasse 12 Altstaetten 9450 CH Other 510(k) Applications for this Company
Contact	Marina Hess Other 510(k) Applications for this Contact
Regulation Number	888.3060   More FDA Info for this Regulation Number
Classification Product Code	MQP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/30/2020
Decision Date	05/29/2020
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