TITANIUM MESH MAXILLOFACIAL IMPLANT SYSTEM— 510(k) K896369

Name: FDA 510(k) clearance K896369
Creator: U.S. Food and Drug Administration
Published: 1989-11-24

Substantially Equivalent

Techmedica, Inc.

FDA 510(k) clearance K896369 for TITANIUM MESH MAXILLOFACIAL IMPLANT SYSTEM, Substantially Equivalent on 1989-11-24. Applicant: Techmedica, Inc.. Device class: 2.

Clearance details

Applicant: Techmedica, Inc.
Product code: Code EZX
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1989-11-06
Decision date: 1989-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EZX

view all

K063461 — ANOVA CONTAINMENT DEVICE2009-08-13
K014200 — OPTIMESH2003-11-26
K032344 — THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-3302003-10-02
K032282 — MODIFICATION TO HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM2003-08-21
K024169 — MACROPORE OS RECONSTRUCTION2003-07-01

More clearances from Techmedica, Inc.

view all

K933935 — CKS POROUS COATED FEMORAL COMPONENT1994-10-11
K932017 — TECHMEDICA CONTINUUM HIP WITH HA COATING1994-09-01
K931929 — TECHMEDICA CONTINUUM HIP SYSTEM1994-03-29
K926387 — TECHMEDICA STANDARD CEMENTED HIP SYSTEM1994-02-01
K925420 — TECHMEDICA STANDARD BIPOLAR SYSTEM1993-09-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.