510(k) K240113— CORIOGRAPH Knee Pre-Op Plan

Substantially Equivalent

Smith & Nephew, Inc.

Clearance details

Applicant: Smith & Nephew, Inc.
Product code: Code PBF
Advisory panel: Orthopedic
Date received: 2024-01-16
Decision date: 2024-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Memphis, TN, US

Adverse events under product code PBF

product code PBF

Injury: 180
Total: 180

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.