Medtronic DUET External Drainage and Monitoring System— 510(k) DEN120017
UnknownMedtronic Neurosurgery
FDA 510(k) clearance DEN120017 for Medtronic DUET External Drainage and Monitoring System, Unknown on 2014-08-22. Applicant: Medtronic Neurosurgery.
Clearance details
- Applicant
- Medtronic Neurosurgery
- Product code
- Code PCB
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Goleta, CA, US
Adverse events under product code PCB
product code PCB- Other
- 1
- Total
- 1
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.