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FDA Product Code

FDA Product Code EZX — Clearance Directory

Device Class
Class II
21 CFR Citation
878.3300

510(k) Clearances — 12 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K063461 ANOVA CONTAINMENT DEVICE Anova Corporation 2009-08-13 Traditional PDF ↗
K014200 OPTIMESH Spineology, Inc. 2003-11-26 Traditional PDF ↗
K032344 THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330 Implex Corp. 2003-10-02 Special PDF ↗
K032282 MODIFICATION TO HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM Implex Corp. 2003-08-21 Special PDF ↗
K024169 MACROPORE OS RECONSTRUCTION Macropore Biosurgery, Inc. 2003-07-01 Traditional PDF ↗
K023882 THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM Implex Corp. 2003-02-19 Traditional PDF ↗
K020853 NUVASIVE MESH Nuvasive, Inc. 2002-06-13 Traditional PDF ↗
K983766 SYNTHES SYNMESH Synthes (Usa) 1998-12-18 Traditional PDF ↗
K945027 TROCHANTER MESH Acu Med, Inc. 1995-02-01 Traditional PDF ↗
K900138 MOTECH TITANIUM SURGICAL MESH Biedermann Motech GmbH 1990-03-20 Traditional PDF ↗
K896369 TITANIUM MESH MAXILLOFACIAL IMPLANT SYSTEM Techmedica, Inc. 1989-11-24 Traditional PDF ↗
K890601 STUART TITANIUM SURGICAL MESH Stuart 1989-03-16 Traditional PDF ↗

Product code EZX · Class II · General, Plastic Surgery. Data: openFDA.