The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Thp Hip Fracture Plating System.
| Device ID | K173826 |
| 510k Number | K173826 |
| Device Name: | THP Hip Fracture Plating System |
| Classification | Device, Fixation, Proximal Femoral, Implant |
| Applicant | Biomet, Inc. 56 East Bell Drive Warsaw, IN 46582 |
| Contact | Annette Minthorn |
| Correspondent | Annette Minthorn Biomet, Inc. 56 East Bell Drive Warsaw, IN 46582 |
| Product Code | JDO |
| Subsequent Product Code | HWC |
| Subsequent Product Code | KTT |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-18 |
| Decision Date | 2018-02-07 |
| Summary: | summary |