Anatomic PEEK Cervical Fusion System with Nanotechnology— 510(k) K230936

Name: FDA 510(k) clearance K230936
Creator: U.S. Food and Drug Administration
Published: 2023-06-02

Substantially Equivalent

Nanovis, LLC

FDA 510(k) clearance K230936 for Anatomic PEEK Cervical Fusion System with Nanotechnology, Substantially Equivalent on 2023-06-02. Applicant: Nanovis, LLC. Device class: 2.

Clearance details

Applicant: Nanovis, LLC
Product code: Code ODP
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2023-04-03
Decision date: 2023-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia City, IN, 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 Nanovis, LLC

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K241605 — Adaptix PEEK Interbody System with Nanotechnology; Capstone Control PEEK Spinal System with Nanotechnology2024-09-05
K203452 — Nano FortiFix® System2020-12-22
K191822 — Nano FortiCore, FortiCore2019-10-11
K171312 — FortiCore®2018-01-22
K161485 — Nanovis Intervertebral Body Fusion System and Forticore(R)2016-09-06

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.