FDA 510(k) Application Details - K092695

Device Classification Name	Appliance, Fixation, Spinal Intervertebral Body   More FDA Info for this Device
510(K) Number	K092695
Device Name	Appliance, Fixation, Spinal Intervertebral Body
Applicant	TRANSCORP, INC. 1000 100TH ST. SW, SUITE F BYRON CENTER, MI US Other 510(k) Applications for this Company
Contact	ANDREW RODENHOUSE 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	09/02/2009
Decision Date	05/21/2010
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