Ti-Largo Cervical Interbody System— 510(k) K223231

Name: FDA 510(k) clearance K223231
Creator: U.S. Food and Drug Administration
Published: 2023-02-24

Substantially Equivalent

Flospine

FDA 510(k) clearance K223231 for Ti-Largo Cervical Interbody System, Substantially Equivalent on 2023-02-24. Applicant: Flospine. Device class: 2.

Clearance details

Applicant: Flospine
Product code: Code ODP
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2022-10-18
Decision date: 2023-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boca Raton, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ODP

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K262595 — VariLift-C Cervical Interbody Fusion System2026-08-26
K262489 — BluEX Cervical Expandable Cage System2026-08-18
K253041 — 3d Cage Cervical2026-07-23
K262061 — Tritanium® C Anterior Cervical Cage +16 more2026-07-17
K254130 — C.A. Medical Interbody Fusion System2026-07-08

More clearances from Flospine

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K232484 — KeyLift Expandable Interlaminar Stabilization System2023-10-19
K210182 — PANAMA Anterior Cervical Plate (ACP) System2021-04-07
K141850 — FLOSPINE PEDICLE SCREW SYSTEM2014-10-27

Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

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.