FDA 510(k) Application Details - K051320

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Solid-Sphere, Lumbar   More FDA Info for this Device
510(K) Number	K051320
Device Name	Intervertebral Fusion Device With Bone Graft, Solid-Sphere, Lumbar
Applicant	MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE MEMPHIS, TN 38132 US Other 510(k) Applications for this Company
Contact	RICHARD W TREHARNE Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	NVR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/20/2005
Decision Date	09/09/2005
Decision	SESU - SE - WITH LIMITATIONS
Classification Advisory Committee	-
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review