The following data is part of a premarket notification filed by Orthopediatrics, Corp with the FDA for Orthopediatrics Pedifoot Deformity Corrections System.
| Device ID | K190992 |
| 510k Number | K190992 |
| Device Name: | OrthoPediatrics PediFoot Deformity Corrections System |
| Classification | Plate, Fixation, Bone |
| Applicant | OrthoPediatrics, Corp 2850 Frontier Drive Warsaw, IN 46582 |
| Contact | Jen Gregory |
| Correspondent | Jen Gregory OrthoPediatrics, Corp 2850 Frontier Drive Warsaw, IN 46582 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-04-15 |
| Decision Date | 2019-08-06 |