FDA 510(k) Applications Submitted by DAVE LAMB

FDA 510(k) Number	Submission Date	Device Name	Applicant
K100008	01/04/2010	CARDO MEDICAL CERAMIC HIP SYSTEM	CARDO MEDICAL, INC
K150812	03/26/2015	Genesys Spine Apache Cervical Interbody Fusion System	Genesys Spine
K161404	05/20/2016	Genesys Spine Apache« Lateral Lumbar Interbody Fusion System	Genesys Spine
K132122	07/10/2013	KESTREL POSTERIOR CERVICAL SPINE SYSTEM	OMNI SURGICAL LLC DBA SPINE360
K122085	07/16/2012	STINGRAY CERVICAL CAGE	OMNI SURGICAL, LP DBA SPINE360
K203003	10/01/2020	Pantheon IBFD	Pantheon Spinal
K102995	10/08/2010	TALON SPINAL SYSTEM	SPINE360
K153123	10/29/2015	Genesys Spine Apache Interbody Fusion System	GENESYS SPINE
K094045	12/31/2009	MODIFICAITON TO: CARDO MEDICAL HIP SYSTEM	CARDO MEDICAL CORP.
K020583	02/21/2002	IVD GIARDIA ANTIGEN DETECTION ASSAY MODEL GL-96	IVD RESEARCH, INC.
K031059	03/28/2003	IVD CRYPTOSPORIDIUM ANTIGEN DETECTION ASSAY, MODEL CP-96	IVD RESEARCH, INC.
K032897	09/17/2003	C. DIFFICILE TOXIN A + B FECAL ANTIGEN DETECTION MICROWELL ELISA KIT MODEL; CDIFF-96	IVD RESEARCH, INC.
K024113	12/13/2002	IVD CRYPTO/GIARDIA DFA	IVD RESEARCH, INC.