The following data is part of a premarket notification filed by Biomet Inc. with the FDA for A. L. P. S. Clavicle Plating System.
| Device ID | K173767 |
| 510k Number | K173767 |
| Device Name: | A. L. P. S. Clavicle Plating System |
| Classification | Plate, Fixation, Bone |
| Applicant | Biomet Inc. 56 East Bell Drive Warsaw, IN 46582 |
| Contact | Dhaval Saraiya |
| Correspondent | Dhaval Saraiya Biomet Inc. 56 East Bell Drive 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 | 2017-12-11 |
| Decision Date | 2018-04-06 |
| Summary: | summary |