K251718

Substantially Equivalent

ArTT Augments and Buttresses and Bone Screws

Applicant: Lima Corporate S.P.A.
Product code: LPH
Advisory panel: Orthopedic
Date received: 2025-06-04
Decision date: 2025-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Villanova Di San Daniele, IT

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.