ANCHOR-L LUMBAR CAGE— 510(k) K120869

Substantially Equivalent

Stryker Spine

FDA 510(k) clearance K120869 for ANCHOR-L LUMBAR CAGE, Substantially Equivalent on 2012-10-25. Applicant: Stryker Spine.

Clearance details

Applicant: Stryker Spine
Product code: Code OVD
Advisory panel: Orthopedic
Date received: 2012-03-22
Decision date: 2012-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Allendale, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OVD

product code OVD

Death: 5
Injury: 495
Total: 500

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.