ROSA® Shoulder System— 510(k) K233199

Substantially Equivalent

Orthosoft Inc (D/B/A Zimmer Cas)

FDA 510(k) clearance K233199 for ROSA® Shoulder System, Substantially Equivalent on 2024-02-21. Applicant: Orthosoft Inc (D/B/A Zimmer Cas).

Clearance details

Applicant: Orthosoft Inc (D/B/A Zimmer Cas)
Product code: Code OLO
Advisory panel: Neurology
Date received: 2023-09-28
Decision date: 2024-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code OLO

product code OLO

Death: 11
Injury: 2,799
Malfunction: 11,105
Other: 1
Total: 13,916

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.