OSS-BODIES PROXIMAL TIBIAL SLEEVE— 510(k) K060131

Name: FDA 510(k) clearance K060131
Creator: U.S. Food and Drug Administration
Published: 2006-02-15

Substantially Equivalent

Biomet Manufacturing Corp

FDA 510(k) clearance K060131 for OSS-BODIES PROXIMAL TIBIAL SLEEVE, Substantially Equivalent on 2006-02-15. Applicant: Biomet Manufacturing Corp. Device class: 2.

Clearance details

Applicant: Biomet Manufacturing Corp
Product code: Code KRO
Device class: Class 2
Regulation: 21 CFR 888.3510
Advisory panel: Orthopedic
Date received: 2006-01-18
Decision date: 2006-02-15
Decision: Substantially Equivalent
Clearance type: Special
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

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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.