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 |