FDA 510(k) Application Details - K081332

Device Classification Name	Spinal Vertebral Body Replacement Device   More FDA Info for this Device
510(K) Number	K081332
Device Name	Spinal Vertebral Body Replacement Device
Applicant	SIGNUS MEDIZINTECHNIK GMBH 8202 SHERMAN ROAD CHSETERLAND, OH 44026 US Other 510(k) Applications for this Company
Contact	KAREN E WARDEN Other 510(k) Applications for this Contact
Regulation Number	888.3060   More FDA Info for this Regulation Number
Classification Product Code	MQP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/12/2008
Decision Date	06/10/2008
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