Biomet Bone Cement R— 510(k) K172408

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K172408 for Biomet Bone Cement R, Substantially Equivalent on 2017-10-05. Applicant: Biomet, Inc..

Clearance details

Applicant: Biomet, Inc.
Product code: Code LOD
Advisory panel: Orthopedic
Date received: 2017-08-09
Decision date: 2017-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

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Adverse events under product code LOD

product code LOD

Death: 44
Injury: 3,004
Malfunction: 895
Other: 4
Total: 3,947

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.