FDA 510(k) Application Details - K162351

Device Classification Name	More FDA Info for this Device
510(K) Number	K162351
Device Name	SeaSpine« Vu aòPODÖ Prime NanoMetalene« Intervertebral Body Fusion Device
Applicant	SEASPINE ORTHOPEDICS CORPORATION 5770 ARMADA DRIVE CARLSBAD, CA 92008 US Other 510(k) Applications for this Company
Contact	Gina Flores Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OVD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/23/2016
Decision Date	12/01/2016
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