Neoss Ti Reinforced Membrane— 510(k) K143327

Substantially Equivalent

Neoss, Ltd.

FDA 510(k) clearance K143327 for Neoss Ti Reinforced Membrane, Substantially Equivalent on 2015-04-13. Applicant: Neoss, Ltd.. Device class: 2.

Clearance details

Applicant: Neoss, Ltd.
Product code: Code NPK
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2014-11-20
Decision date: 2015-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Harrogate, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code NPK

K221851 — Lumina-PTFE Titanium2023-12-08
K222549 — OpenTex2023-05-11
K211554 — InnoGenic Non-resorbable Membrane2023-02-24
K210797 — Bio-MEM Ti Reinforced Membrane2022-08-18
K201187 — Cytoplast Titanium-Reinforced PTFE Membranes2021-01-23

More clearances from Neoss, Ltd.

K211396 — Neoss Individual Prosthetics2022-05-17
K150669 — Neoss TiBase, Neoss CoCr Abutments (Mono and Multi)2015-10-08
K113376 — NEOSS PROACTIVE TAPERED IMPLANT2012-09-05
K090452 — NEOSS IMPLANT SYSTEM 03.252009-05-22
K081851 — NEOSS ACCESS ABUTMENTS2009-03-02

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