FDA 510(k) Application Details - K090316

Device Classification Name	Appliance, Fixation, Spinal Intervertebral Body   More FDA Info for this Device
510(K) Number	K090316
Device Name	Appliance, Fixation, Spinal Intervertebral Body
Applicant	LANX, INC. 390 INTERLOCKEN CRESCENT SUITE 890 BROOMFIELD, CO 80021 US Other 510(k) Applications for this Company
Contact	ANDREW LAMBORNE Other 510(k) Applications for this Contact
Regulation Number	888.3060   More FDA Info for this Regulation Number
Classification Product Code	KWQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/09/2009
Decision Date	04/07/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review