FDA 510(k) Applications for Medical Device Product Code "EZX"
(Mesh, Metal)

FDA 510(k) Number Applicant Device Name Decision Date
K945027 ACUMED, INC. TROCHANTER MESH 02/01/1995
K063461 ANOVA CORPORATION ANOVA CONTAINMENT DEVICE 08/13/2009
K900138 BIEDERMANN MOTECH GMBH MOTECH TITANIUM SURGICAL MESH 03/20/1990
K032282 IMPLEX CORP. MODIFICATION TO HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM 08/21/2003
K023882 IMPLEX CORP. THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM 02/19/2003
K032344 IMPLEX CORP. THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330 10/02/2003
K024169 MACROPORE BIOSURGERY, INC. MACROPORE OS RECONSTRUCTION 07/01/2003
K020853 NUVASIVE, INC. NUVASIVE MESH 06/13/2002
K014200 SPINEOLOGY, INC. OPTIMESH 11/26/2003
K890601 STUART STUART TITANIUM SURGICAL MESH 03/16/1989
K983766 SYNTHES (USA) SYNTHES SYNMESH 12/18/1998
K896369 TECHMEDICA, INC. TITANIUM MESH MAXILLOFACIAL IMPLANT SYSTEM 11/24/1989


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