Entasis 3D Dual-Lead Sacroiliac Implant System— 510(k) K223708

Substantially Equivalent

Corelink, LLC

FDA 510(k) clearance K223708 for Entasis 3D Dual-Lead Sacroiliac Implant System, Substantially Equivalent on 2023-03-21. Applicant: Corelink, LLC.

Clearance details

Applicant: Corelink, LLC
Product code: Code OUR
Advisory panel: Orthopedic
Date received: 2022-12-12
Decision date: 2023-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OUR

product code OUR

Death: 3
Injury: 347
Total: 350

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.