Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FRAXION Spinal Fixation System

K-Number: K262091 · 2026-09-17

ApplicantOrtler Global Tibbi Gerecler Anonim Sirketi
Decision Date2026-09-17
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FRAXION Spinal Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Ortler Global Tibbi Gerecler Anonim Sirketi. It received FDA 510(k) clearance on 2026-09-17 under 510(k) number K262091. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRAXION Spinal Fixation System?

FRAXION Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2026-09-17. The listed applicant is Ortler Global Tibbi Gerecler Anonim Sirketi. The 510(k) number is K262091.

When did FRAXION Spinal Fixation System receive FDA 510(k) clearance?

FRAXION Spinal Fixation System received FDA 510(k) clearance on 2026-09-17, under 510(k) number K262091.

Who is the listed applicant for FRAXION Spinal Fixation System?

The FDA 510(k) record lists Ortler Global Tibbi Gerecler Anonim Sirketi as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FRAXION Spinal Fixation System?

The FDA product code for FRAXION Spinal Fixation System is NKB.

Other records listing Ortler Global Tibbi Gerecler Anonim Sirketi as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261830FRAXION 3.5 Plate System (Various - See Catalog);FRAXION 4.5 Plate System (Various - See Catalog);FRAXION Mini Plate System (Various - See Catalog);FRAXION Bone Screw System (Various - See Catalog)

Related Devices (Code: NKB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262193RIVA® Posterior Fixation System with NanoACTIV Surface Technology; RIVA® Anchor Sacroiliac Fixation System with NanoACTIV Surface TechnologyXenix MedicalK262828KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.OK260362QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)MANTIZ Co., Ltd.K253943Tiger 2 SystemZavation Medical Products, LLCK261284Invictus® Small Stature Spinal Fixation System; Invictus® 2.0 Spinal Fixation SystemAlphatec Spine, Inc.K253802KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.O

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑