FDA 510(k) Applications Submitted by SURESH GHAI

FDA 510(k) Number	Submission Date	Device Name	Applicant
K110045	01/06/2011	INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE	VERTEBRAL TECHNOLOGIES, INC.
K110226	01/25/2011	INTERFUSE T INVERTEBRAL BODY FUSION DEVICE	VERTEBRAL TECHNOLOGIES, INC.
K131540	05/29/2013	INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE	VERTEBRAL TECHNOLOGIES, INC.
K091988	07/02/2009	MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076	VERTEBRAL TECHNOLOGIES, INC.
K102277	08/11/2010	INTERFUSE T INVERTEBRAL BODY FUSION DEVICE	VERTEBRAL TECHNOLOGIES, INC.
K093675	11/27/2009	INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076	VERTEBRAL TECHNOLOGIES, INC.