P.F.C. APICAL PLUG— 510(k) K944769

Name: FDA 510(k) clearance K944769
Creator: U.S. Food and Drug Administration
Published: 1994-12-08

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K944769 for P.F.C. APICAL PLUG, Substantially Equivalent on 1994-12-08. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 3.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code JDL
Device class: Class 3
Regulation: 21 CFR 888.3320
Advisory panel: Orthopedic
Date received: 1994-09-27
Decision date: 1994-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: King Of Prussia, PA, US

Download summary PDF View on FDA.gov ↗

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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.