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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.
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