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 |