The following data is part of a premarket notification filed by Biomet Inc with the FDA for Biomet Variable Pitch Compression Screw System.
| Device ID | K160058 |
| 510k Number | K160058 |
| Device Name: | Biomet Variable Pitch Compression Screw System |
| Classification | Screw, Fixation, Bone |
| Applicant | Biomet Inc 56 East Bell Drive Warsaw, IN 46582 |
| Contact | Julie Largent |
| Correspondent | Julie Largent Biomet Inc 56 East Bell Drive Warsaw, IN 46582 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-01-12 |
| Decision Date | 2016-03-09 |
| Summary: | summary |