The following data is part of a premarket notification filed by Orthofix Srl with the FDA for Sole Medial Column Fusion Plate.
| Device ID | K210157 |
| 510k Number | K210157 |
| Device Name: | SOLE Medial Column Fusion Plate |
| Classification | Plate, Fixation, Bone |
| Applicant | Orthofix SRL Via Delle Nazioni, 9 Bussolengo, IT 37012 |
| Contact | Gianluca Ricadona |
| Correspondent | Cheryl Wagoner Wagoner Consulting LLC PO Box 15729 Wilmington, NC 28408 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-01-21 |
| Decision Date | 2021-04-20 |
| Summary: | summary |