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 |