MODIFICATION TO: DSS STABILIZATION SYSTEM— 510(k) K090408

Unknown

Paradigm Spine, LLC

FDA 510(k) clearance K090408 for MODIFICATION TO: DSS STABILIZATION SYSTEM, Unknown on 2009-03-20. Applicant: Paradigm Spine, LLC.

Clearance details

Applicant: Paradigm Spine, LLC
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2009-02-18
Decision date: 2009-03-20
Decision: Unknown
Clearance type: Special
Location: Washington, DC, 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.