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FDA 510(k) Applications for Medical Device Product Code "EZX"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K063461 | ANOVA CORPORATION | ANOVA CONTAINMENT DEVICE | 08/13/2009 |
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 |
K983766 | SYNTHES (USA) | SYNTHES SYNMESH | 12/18/1998 |