DSS STABILIZATION SYSTEM— 510(k) K113625
UnknownParadigm Spine, LLC
FDA 510(k) clearance K113625 for DSS STABILIZATION SYSTEM, Unknown on 2012-01-10. Applicant: Paradigm Spine, LLC.
Clearance details
- Applicant
- Paradigm Spine, LLC
- Product code
- Code NKB
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Special
- Location
- Washington, DC, US
Adverse events under product code NKB
product code NKB- Death
- 27
- Injury
- 5,033
- Malfunction
- 4,140
- Total
- 9,200
Source: openFDA MAUDE database, through . 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.