K922308

Substantially Equivalent

TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER

Applicant: Ti-Mesh, Inc.
Product code: FTM
Advisory panel: General, Plastic Surgery
Date received: 1992-05-15
Decision date: 1993-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Las Vegas, NV, US

Adverse events under product code FTM

product code FTM

Death: 17
Injury: 2,174
Total: 2,191

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.