CONVENTUS DRS— 510(k) K131552

Substantially Equivalent

Conventus Orthopaedics

FDA 510(k) clearance K131552 for CONVENTUS DRS, Substantially Equivalent on 2014-02-12. Applicant: Conventus Orthopaedics.

Clearance details

Applicant: Conventus Orthopaedics
Product code: Code HRS
Advisory panel: Orthopedic
Date received: 2013-05-30
Decision date: 2014-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Maple Grove, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HRS

product code HRS

Death: 27
Injury: 10,340
Malfunction: 3,328
Total: 13,695

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.