VERTICOR K-WIRE SYSTEM— 510(k) K110047

Name: FDA 510(k) clearance K110047
Creator: U.S. Food and Drug Administration
Published: 2011-02-28

Substantially Equivalent

Verticor, Ltd.

FDA 510(k) clearance K110047 for VERTICOR K-WIRE SYSTEM, Substantially Equivalent on 2011-02-28. Applicant: Verticor, Ltd.. Device class: 2.

Clearance details

Applicant: Verticor, Ltd.
Product code: Code HTY
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 2011-01-06
Decision date: 2011-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Round Rock, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

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.