| Device |
implant, subperiosteal |
| Regulation Description |
Subperiosteal implant material. |
| Regulation Medical Specialty |
Dental |
| Review Panel |
Dental |
| Product Code | ELE |
| Premarket Review |
Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices
(OHT1)
Division of Dental and ENT Devices
(DHT1B)
|
| Submission Type |
510(k)
|
| Regulation Number |
872.3645
|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
Summary Malfunction Reporting |
Eligible |
| Implanted Device? |
Yes
|
| Life-Sustain/Support Device? |
No
|
| Recognized Consensus Standards
|
| Third Party Review |
Not Third Party Eligible |
|
|