| Device |
external cerebrospinal fluid (csf) diversion |
| Regulation Description |
Cerebrospinal fluid shunt system. |
| Definition |
Cerebrospinal fluid (CSF) diversion intended to alter spinal cord perfusion. |
| Physical State |
CSF drainage system. |
| Technical Method |
Diverts CSF in order to alter spinal cord perfusion pressures. |
| Target Area |
Central nervous system (CNS) subarachnoid and ventricular space. |
| Regulation Medical Specialty |
Neurology |
| Review Panel |
Neurology |
| Product Code | PCB |
| Premarket Review |
Office of Neurological and Physical Medicine Devices
(OHT5)
Neurosurgical, Neurointerventional and Neurodiagnostic Devices
(DHT5A)
|
| Submission Type |
510(k)
|
| Regulation Number |
882.5560
|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
Summary Malfunction Reporting |
Ineligible |
| Implanted Device? |
No
|
| Life-Sustain/Support Device? |
No
|
| Recognized Consensus Standard
|
| Third Party Review |
Not Third Party Eligible |