P.F.C. HIP SYSTEM NON-POROUS ACETABULAR COMPONENT— 510(k) K902137

Substantially Equivalent

Johnson & Johnson Orthopaedics, Inc.

FDA 510(k) clearance K902137 for P.F.C. HIP SYSTEM NON-POROUS ACETABULAR COMPONENT, Substantially Equivalent on 1990-06-26. Applicant: Johnson & Johnson Orthopaedics, Inc..

Clearance details

Applicant: Johnson & Johnson Orthopaedics, Inc.
Product code: Code JDI
Advisory panel: Orthopedic
Date received: 1990-05-11
Decision date: 1990-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Braintree, MA, US

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Adverse events under product code JDI

product code JDI

Death: 65
Injury: 12,943
Malfunction: 1,681
Total: 14,689

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.