Pantheon Proximal Femur Reconstruction (PFR) System— 510(k) K241059

Substantially Equivalent

Adler Ortho S.P.A

FDA 510(k) clearance K241059 for Pantheon Proximal Femur Reconstruction (PFR) System, Substantially Equivalent on 2025-01-13. Applicant: Adler Ortho S.P.A.

Clearance details

Applicant: Adler Ortho S.P.A
Product code: Code LPH
Advisory panel: Orthopedic
Date received: 2024-04-18
Decision date: 2025-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cormano (Mi), IT

Download summary PDF View on FDA.gov ↗

Adverse events under product code LPH

product code LPH

Death: 73
Injury: 31,640
Malfunction: 3,358
Other: 2
Total: 35,073

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.