PEDIATRIC FIXATION RODS— 510(k) K000764

Name: FDA 510(k) clearance K000764
Creator: U.S. Food and Drug Administration
Published: 2000-04-06

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K000764 for PEDIATRIC FIXATION RODS, Substantially Equivalent on 2000-04-06. Applicant: Biomet, Inc.. Device class: 2.

Clearance details

Applicant: Biomet, Inc.
Product code: Code JDS
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 2000-03-09
Decision date: 2000-04-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Warsaw, IN, 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.