FDA 510(k) Application Details - K122588

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Cervical   More FDA Info for this Device
510(K) Number	K122588
Device Name	Intervertebral Fusion Device With Bone Graft, Cervical
Applicant	ORTHO DEVELOPMENT CORP. 12187 SOUTH BUSINESS PARK DR. DRAPER, UT 84020 US Other 510(k) Applications for this Company
Contact	TOM HAUETER 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	08/24/2012
Decision Date	06/12/2013
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