| Device Classification Name |
plate, fixation, bone |
|||
|---|---|---|---|---|
| 510(k) Number | K131474 | |||
| Device Name | ARTHREX DISTAL RADIUS PLATE SYSTEM | |||
| Applicant |
|
|||
| Applicant Contact | courtney smith | |||
| Correspondent |
|
|||
| Correspodent Contact | courtney smith | |||
| Regulation Number | 888.3030 | |||
| Classification Product Code |
|
|||
| Subsequent Product Code |
|
|||
| Date Received | 05/22/2013 | |||
| Decision Date | 07/03/2013 | |||
| Decision |
substantially equivalent (SESE) |
|||
| Regulation Medical Specialty |
Orthopedic |
|||
| 510k Review Panel |
Orthopedic |
|||
| summary |
summary |
|||
| Type | Traditional | |||
| Reviewed by Third Party | No | |||
| Combination Product |
No |