XIA 4.5 SPINAL SYSTEM— 510(k) K121342

Unknown

Stryker Corp.

FDA 510(k) clearance K121342 for XIA 4.5 SPINAL SYSTEM, Unknown on 2012-06-22. Applicant: Stryker Corp..

Clearance details

Applicant: Stryker Corp.
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2012-05-04
Decision date: 2012-06-22
Decision: Unknown
Clearance type: Traditional
Location: Allendale, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code NKB

product code NKB

Death: 27
Injury: 5,033
Malfunction: 4,140
Total: 9,200

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.