The following data is part of a premarket notification filed by Orthopediatrics, Corp. with the FDA for Pediatric Nailing Platformfemur.
| Device ID | K190321 |
| 510k Number | K190321 |
| Device Name: | Pediatric Nailing PlatformFemur |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| 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 | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-02-13 |
| Decision Date | 2019-10-09 |
| Summary: | summary |