The following data is part of a premarket notification filed by Biomet Manufacturing with the FDA for Biomet Proximal Humerus Plating System.
| Device ID | K143697 |
| 510k Number | K143697 |
| Device Name: | Biomet Proximal Humerus Plating System |
| Classification | Plate, Fixation, Bone |
| Applicant | Biomet Manufacturing 56 East Bell Drive, PO Box 587 Warsaw, IN 46582 |
| Contact | Julie Largent |
| Correspondent | Julie Largent Biomet Manufacturing 56 East Bell Drive, PO Box 587 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 | 2014-12-24 |
| Decision Date | 2015-03-30 |
| Summary: | summary |