TRIATHLON SCREW-FIXATION TIBIAL BASEPLATE— 510(k) K072575

Name: FDA 510(k) clearance K072575
Creator: U.S. Food and Drug Administration
Published: 2008-01-07

Substantially Equivalent

Stryker Orthopaedics

FDA 510(k) clearance K072575 for TRIATHLON SCREW-FIXATION TIBIAL BASEPLATE, Substantially Equivalent on 2008-01-07. Applicant: Stryker Orthopaedics. Device class: 2.

Clearance details

Applicant: Stryker Orthopaedics
Product code: Code MBH
Device class: Class 2
Regulation: 21 CFR 888.3565
Advisory panel: Orthopedic
Date received: 2007-09-13
Decision date: 2008-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mahwah, NJ, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MBH

product code MBH

Injury: 6,545
Malfunction: 2,023
Total: 8,568

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.