FDA 510(k) Application Details - K123207

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Lumbar   More FDA Info for this Device
510(K) Number	K123207
Device Name	Intervertebral Fusion Device With Bone Graft, Lumbar
Applicant	OSTEOMED LP 3885 Arapaho Rd ADDISON, TX 75001 US Other 510(k) Applications for this Company
Contact	PIEDAD PENA 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	10/12/2012
Decision Date	11/29/2012
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