ACTIFY Unicondylar Knee System— 510(k) K241260
Substantially EquivalentGlobus Medical, Inc.
FDA 510(k) clearance K241260 for ACTIFY Unicondylar Knee System, Substantially Equivalent on 2024-12-06. Applicant: Globus Medical, Inc..
Clearance details
- Applicant
- Globus Medical, Inc.
- Product code
- Code HSX
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Audubon, PA, US
Adverse events under product code HSX
product code HSX- Injury
- 1,003
- Other
- 1
- Total
- 1,004
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.