Anterior Cervical Plate System— 510(k) K202972

Name: FDA 510(k) clearance K202972
Creator: U.S. Food and Drug Administration
Published: 2020-11-24

Substantially Equivalent

Nutech Spine and Biologics

FDA 510(k) clearance K202972 for Anterior Cervical Plate System, Substantially Equivalent on 2020-11-24. Applicant: Nutech Spine and Biologics. Device class: 2.

Clearance details

Applicant: Nutech Spine and Biologics
Product code: Code KWQ
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2020-09-30
Decision date: 2020-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Birmingham, AL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KWQ

view all

K261309 — Palisades Buttress Plate System2026-07-16
K252776 — ARIES Anterior Cervical Plate Systems2026-05-14
K261112 — CastleLoc-P Anterior Cervical Plate System2026-05-06
K260570 — corra cervical plating system2026-04-22
K260697 — VyPlate Anterior Cervical Plate System2026-03-27

Adverse events under product code KWQ

product code KWQ

Death: 8
Injury: 1,212
Malfunction: 1,233
Total: 2,453

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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