| Device Type ID | 3845 |
| Device Name | Inhibitor, Peridural Fibrosis (adhesion Barrier) |
| Review Panel | Neurology |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Neurological And Physical Medicine Devices (DNPMD) Physical Medicine And Rehabilitation Devices Branch (PMDB) |
| Submission Type | PMA |
| FDA Device Classification | Class 3 Medical Device |
| Product Code | MLQ |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 3845 |
| Device | Inhibitor, Peridural Fibrosis (adhesion Barrier) |
| Product Code | MLQ |
| FDA Device Classification | Class 3 Medical Device |