SELF-ALIGNING ACETABULAR COMPONENT— 510(k) K831792

Name: FDA 510(k) clearance K831792
Creator: U.S. Food and Drug Administration
Published: 1984-09-20

Substantially Equivalent

Endomedics, Inc.

FDA 510(k) clearance K831792 for SELF-ALIGNING ACETABULAR COMPONENT, Substantially Equivalent on 1984-09-20. Applicant: Endomedics, Inc.. Device class: 3.

Clearance details

Applicant: Endomedics, Inc.
Product code: Code JDL
Device class: Class 3
Regulation: 21 CFR 888.3320
Advisory panel: Orthopedic
Date received: 1983-06-03
Decision date: 1984-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K842202 — NEW JERSEY ACETABULAR COMPONENT &1984-07-20
K842233 — NEW JERSEY FEMORAL RESURFACING COMPONENT1984-07-20
K842234 — NEW JERSEY FEMORAL STEM1984-07-20

Adverse events under product code JDL

product code JDL

Injury: 285
Total: 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.