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 |