Product code EZX— General, Plastic Surgery
ANOVA CONTAINMENT DEVICE
- Classification name
- Mesh, Surgical, Metal
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 12
- First cleared
- Most recent
Market context for product code EZX
FDA has cleared devices under product code EZX between 1989 and 2009, filed by 10 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2009
- 2003
- 2002
- 1998
- 1995
- 1990
- 1989
Top applicants under product code EZX
Recent clearances under product code EZX
- K063461 — ANOVA CONTAINMENT DEVICE
- K014200 — OPTIMESH
- K032344 — THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330
- K032282 — MODIFICATION TO HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM
- K024169 — MACROPORE OS RECONSTRUCTION
- K023882 — THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM
- K020853 — NUVASIVE MESH
- K983766 — SYNTHES SYNMESH
- K945027 — TROCHANTER MESH
- K900138 — MOTECH TITANIUM SURGICAL MESH
- K896369 — TITANIUM MESH MAXILLOFACIAL IMPLANT SYSTEM
- K890601 — STUART TITANIUM SURGICAL MESH
Data sourced from openFDA. This site is unofficial and independent of the FDA.