INTRAMEDULLARY BONE PLUG— 510(k) K832328

Name: FDA 510(k) clearance K832328
Creator: U.S. Food and Drug Administration
Published: 1983-10-20

Substantially Equivalent

Kirschner Medical Corp.

FDA 510(k) clearance K832328 for INTRAMEDULLARY BONE PLUG, Substantially Equivalent on 1983-10-20. Applicant: Kirschner Medical Corp.. Device class: 2.

Clearance details

Applicant: Kirschner Medical Corp.
Product code: Code JDS
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 1983-07-15
Decision date: 1983-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JDS

product code JDS

Injury: 1,776
Malfunction: 1,509
Total: 3,285

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.