The following data is part of a premarket notification filed by Orthopediatrics, Corp with the FDA for Orthopediatrics Fracture And Osteotomy Bone Plate System.
Device ID | K111086 |
510k Number | K111086 |
Device Name: | ORTHOPEDIATRICS FRACTURE AND OSTEOTOMY BONE PLATE 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 |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-04-19 |
Decision Date | 2011-06-17 |
Summary: | summary |