The following data is part of a premarket notification filed by Orthopediatrics, Corp. with the FDA for Orthopediatrics Pediloc Tibia Plate System.
Device ID | K100240 |
510k Number | K100240 |
Device Name: | ORTHOPEDIATRICS PEDILOC TIBIA PLATE SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | ORTHOPEDIATRICS, CORP. 210 N. BUFFALO ST. Warsaw, IN 46580 |
Contact | Gary Barnett |
Correspondent | Gary Barnett ORTHOPEDIATRICS, CORP. 210 N. BUFFALO ST. Warsaw, IN 46580 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-01-27 |
Decision Date | 2010-05-17 |
Summary: | summary |