ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM— 510(k) K981230

Substantially Equivalent

Biodynamic Technologies, Inc.

FDA 510(k) clearance K981230 for ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM, Substantially Equivalent on 1998-06-01. Applicant: Biodynamic Technologies, Inc..

Clearance details

Applicant: Biodynamic Technologies, Inc.
Product code: Code HSB
Advisory panel: Orthopedic
Date received: 1998-04-03
Decision date: 1998-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deerfield Beach, FL, US

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Adverse events under product code HSB

product code HSB

Death: 49
Injury: 12,083
Malfunction: 6,561
Other: 1
Total: 18,694

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.