| Device Type ID | 1247 |
| Device Name | Post, Root Canal |
| Regulation Description | Root Canal Post. |
| Regulation Medical Specialty | Dental |
| Review Panel | Dental |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Anesthesiology, General Hospital, Infection Control, And Dental Devices (DAGRID) Dental Devices Branch (DEDB) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 872.3810 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | ELR |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
|
| Device Type ID | 1247 |
| Device | Post, Root Canal |
| Product Code | ELR |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Root Canal Post. |
| CFR Regulation Number | 872.3810 [🔎] |
| Device Problems | |
|---|---|
Break | 7 |
Material Integrity Problem | 3 |
Fracture | 2 |
Device Operates Differently Than Expected | 1 |
Appropriate Term/Code Not Available | 1 |
| Total Device Problems | 14 |
| Recalls | |||
|---|---|---|---|
| Manufacturer | Recall Class | Date Posted | |
| 1 | Coltene Whaledent Inc | II | Nov-02-2018 |