The following data is part of a premarket notification filed by Orthopediatrics, Corp. with the FDA for Pediloc Fragment System.
| Device ID | K140431 |
| 510k Number | K140431 |
| Device Name: | PEDILOC FRAGMENT SYSTEM |
| Classification | Plate, Fixation, Bone |
| Applicant | ORTHOPEDIATRICS, CORP. 2850 FRONTIER DRIVE Warsaw, IN 46582 |
| Contact | Mark Fox |
| Correspondent | Mark Fox ORTHOPEDIATRICS, CORP. 2850 FRONTIER DRIVE Warsaw, IN 46582 |
| Product Code | HRS |
| Subsequent Product Code | HTN |
| Subsequent Product Code | HWC |
| Subsequent Product Code | KTT |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-02-20 |
| Decision Date | 2014-07-29 |
| Summary: | summary |