MAK OSS KNEE FEMORAL COMPONENTS— 510(k) K083779

Substantially Equivalent

Biomet Manufacturing Corp

FDA 510(k) clearance K083779 for MAK OSS KNEE FEMORAL COMPONENTS, Substantially Equivalent on 2009-04-03. Applicant: Biomet Manufacturing Corp.

Clearance details

Applicant: Biomet Manufacturing Corp
Product code: Code KRO
Advisory panel: Orthopedic
Date received: 2008-12-19
Decision date: 2009-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KRO

product code KRO

Death: 19
Injury: 4,841
Total: 4,860

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.