The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Ortholoc 3di Ankle Fusion Plating System.
| Device ID | K121425 |
| 510k Number | K121425 |
| Device Name: | ORTHOLOC 3DI ANKLE FUSION PLATING SYSTEM |
| Classification | Plate, Fixation, Bone |
| Applicant | WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
| Contact | Samir Ibrahim |
| Correspondent | Samir Ibrahim WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-05-14 |
| Decision Date | 2012-10-01 |
| Summary: | summary |