THE UNIVERSAL BONE CEMENT RESISTOR— 510(k) K924323

Substantially Equivalent

Biodynamic Technologies, Inc.

FDA 510(k) clearance K924323 for THE UNIVERSAL BONE CEMENT RESISTOR, Substantially Equivalent on 1993-02-12. Applicant: Biodynamic Technologies, Inc..

Clearance details

Applicant: Biodynamic Technologies, Inc.
Product code: Code JDI
Advisory panel: Orthopedic
Date received: 1992-08-27
Decision date: 1993-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, VA, 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.