AETOS Shoulder System Stemless Humeral Prosthesis— 510(k) K240716

Substantially Equivalent

Smith & Nephew, Inc.

FDA 510(k) clearance K240716 for AETOS Shoulder System Stemless Humeral Prosthesis, Substantially Equivalent on 2024-11-20. Applicant: Smith & Nephew, Inc..

Clearance details

Applicant: Smith & Nephew, Inc.
Product code: Code PKC
Advisory panel: Orthopedic
Date received: 2024-03-15
Decision date: 2024-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cordova, TN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code PKC

product code PKC

Injury: 258
Total: 258

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.