LEVTECH TITANIUM BONE WIRE— 510(k) K910128

Name: FDA 510(k) clearance K910128
Creator: U.S. Food and Drug Administration
Published: 1991-06-18

Substantially Equivalent

Levtech, Inc.

FDA 510(k) clearance K910128 for LEVTECH TITANIUM BONE WIRE, Substantially Equivalent on 1991-06-18. Applicant: Levtech, Inc.. Device class: 2.

Clearance details

Applicant: Levtech, Inc.
Product code: Code JDQ
Device class: Class 2
Regulation: 21 CFR 888.3010
Advisory panel: Orthopedic
Date received: 1991-01-09
Decision date: 1991-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JDQ

product code JDQ

Death: 9
Injury: 330
Total: 339

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.