Skyway Anterior Cervical Plate System— 510(k) K231766

Name: FDA 510(k) clearance K231766
Creator: U.S. Food and Drug Administration
Published: 2023-09-12

Substantially Equivalent

Kyocera Medical Technologies Inc. (KMTI)

FDA 510(k) clearance K231766 for Skyway Anterior Cervical Plate System, Substantially Equivalent on 2023-09-12. Applicant: Kyocera Medical Technologies Inc. (KMTI). Device class: 2.

Clearance details

Applicant: Kyocera Medical Technologies Inc. (KMTI)
Product code: Code KWQ
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2023-06-16
Decision date: 2023-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redlands, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KWQ

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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

More clearances from Kyocera Medical Technologies Inc. (KMTI)

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K260989 — Varion Thoracolumbar Fixation System2026-05-15
K250486 — Skyway Anterior Cervical Plate System2025-04-10

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.