FDA 510(k) Application Details - K150788

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Cervical   More FDA Info for this Device
510(K) Number	K150788
Device Name	Intervertebral Fusion Device With Bone Graft, Cervical
Applicant	MEDITECH SPINE, LLC 1447 PEACHTREE ST NE SUITE 440 ATLANTA, GA 30309 US Other 510(k) Applications for this Company
Contact	Jason Gromek 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	03/25/2015
Decision Date	10/14/2015
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