Rosa Knee System— 510(k) K230180
Substantially EquivalentOrthosoft Inc (D/B/A Zimmer Cas)
FDA 510(k) clearance K230180 for Rosa Knee System, Substantially Equivalent on 2023-02-22. 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
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Montreal, CA
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, through . 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.