KM-2 METAL-BACKED ACETABULAR CUP— 510(k) K844319

Substantially Equivalent for Some Indications

Kirschner Medical Corp.

FDA 510(k) clearance K844319 for KM-2 METAL-BACKED ACETABULAR CUP, Substantially Equivalent for Some Indications on 1985-09-19. Applicant: Kirschner Medical Corp..

Clearance details

Applicant: Kirschner Medical Corp.
Product code: Code JDI
Advisory panel: Orthopedic
Date received: 1984-11-06
Decision date: 1985-09-19
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Plymouth, MN, 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.