NEURO VENTION LAMINPLASTY PLATING SYSTEM— 510(k) K121276

Name: FDA 510(k) clearance K121276
Creator: U.S. Food and Drug Administration
Published: 2012-08-29

Substantially Equivalent

Neurovention, LLC

FDA 510(k) clearance K121276 for NEURO VENTION LAMINPLASTY PLATING SYSTEM, Substantially Equivalent on 2012-08-29. Applicant: Neurovention, LLC. Device class: 2.

Clearance details

Applicant: Neurovention, LLC
Product code: Code NQW
Device class: Class 2
Regulation: 21 CFR 888.3050
Advisory panel: Orthopedic
Date received: 2012-04-27
Decision date: 2012-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Colorado Springs, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NQW

view all

K252930 — AQUA Laminoplasty Systems2026-05-27
K243137 — Curiteva Porous PEEK Laminoplasty System2024-10-28
K242784 — Vy Spine VyLam Laminoplasty System2024-10-16
K232471 — Vy Spine VyLam Laminoplasty System2023-10-10
K231232 — Curiteva Laminoplasty System2023-06-28

More clearances from Neurovention, LLC

view all

K192162 — NeuroVention Cranial Fixation System, NuCrani Plates, KTC Burr Hole Cover, DC Plate2020-03-13

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