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)

VEOFIX Snap Off Screw

K-Number: K253108 · 2026-06-05

ApplicantSteps Ortho
Decision Date2026-06-05
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VEOFIX Snap Off Screw is the device name listed in this FDA 510(k) record. The listed applicant is Steps Ortho. It received FDA 510(k) clearance on 2026-06-05 under 510(k) number K253108. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEOFIX Snap Off Screw?

VEOFIX Snap Off Screw is a medical device that received FDA 510(k) clearance on 2026-06-05. The listed applicant is Steps Ortho. The 510(k) number is K253108.

When did VEOFIX Snap Off Screw receive FDA 510(k) clearance?

VEOFIX Snap Off Screw received FDA 510(k) clearance on 2026-06-05, under 510(k) number K253108.

Who is the listed applicant for VEOFIX Snap Off Screw?

The FDA 510(k) record lists Steps Ortho as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VEOFIX Snap Off Screw?

The FDA product code for VEOFIX Snap Off Screw is HWC. This falls under the Cardiovascular category.

Related Devices (Code: HWC)

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.

K260809Arthrex Sterile VAL and VAL KreuLock™ Compression Screw SystemArthrex, Inc.K261154CoLink® & CoLag® Non-Sterile ScrewsIn2Bones USA, LLCK261241TriMed Compression ScrewsTriMed, Inc.K254215Arthrex Beaming SystemArthrex, Inc.K254077OSSIOfiber® Threaded Trimmable Fixation NailOSSIO , Ltd.K260934TITAN Nail; APTUS K-Wire SystemMedartis AG

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.

↑