GE STERILE ARTHROGRAM TRAY— 510(k) K962035

Substantially Equivalent

GE Medical Systems

FDA 510(k) clearance K962035 for GE STERILE ARTHROGRAM TRAY, Substantially Equivalent on 1996-06-25. Applicant: GE Medical Systems.

Clearance details

Applicant: GE Medical Systems
Product code: Code FMI
Advisory panel: General Hospital
Date received: 1996-05-24
Decision date: 1996-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarpon Springs, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMI

product code FMI

Death: 28
Injury: 1,517
Malfunction: 23,981
Other: 18
Total: 25,544

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.