Biomet Manufacturing, LLC · Class II · Cleared Jun 25, 2015
| K-number | K142814 |
| Device name | Biomet Orthopaedic Salvage System (OSSTM) - Proximal Femoral & Hybrid Tibial |
| Applicant | Biomet Manufacturing, LLC |
| Product code | JDI |
| Device class | Class II |
| Decision date | Jun 25, 2015 |
| Decision | Substantially Equivalent |
| Regulation | 888.3350 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov