FDA 510(k) Application Details - K153495

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Lumbar   More FDA Info for this Device
510(K) Number	K153495
Device Name	Intervertebral Fusion Device With Bone Graft, Lumbar
Applicant	LDR Spine USA 13785 Research Boulevard, Suite 200 Austin, TX 78750 US Other 510(k) Applications for this Company
Contact	Brad Strasser Other 510(k) Applications for this Contact
Regulation Number	888.3080   More FDA Info for this Regulation Number
Classification Product Code	MAX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/07/2015
Decision Date	03/31/2016
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