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 |