The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Tsp Hip Fracture Plating System.
| Device ID | K140018 |
| 510k Number | K140018 |
| Device Name: | TSP HIP FRACTURE PLATING SYSTEM |
| Classification | Device, Fixation, Proximal Femoral, Implant |
| Applicant | BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
| Contact | Gary Baker |
| Correspondent | Gary Baker BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
| Product Code | JDO |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-01-03 |
| Decision Date | 2014-04-04 |
| Summary: | summary |