The following data is part of a premarket notification filed by Orthopediatrics, Inc. with the FDA for Orthopediatrics Pedinail Intramedullary Platform.
| Device ID | K172583 |
| 510k Number | K172583 |
| Device Name: | OrthoPediatrics PediNail Intramedullary Platform |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| Applicant | OrthoPediatrics, Inc. 2850 Frontier Drive Warsaw, IN 46582 |
| Contact | Adam Cargill |
| Correspondent | James L. Crumley OrthoPediatrics, Inc. 2850 Frontier Drive Warsaw, IN 46582 |
| Product Code | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-08-28 |
| Decision Date | 2018-05-10 |
| Summary: | summary |