Wrightmedicaltechnologyinc · Class II · Cleared Mar 13, 2017
| K-number | K163039 |
| Device name | ORTHOLOC® 3Di Small Bones Plating |
| Applicant | Wrightmedicaltechnologyinc |
| Product code | HRS |
| Device class | Class II |
| Decision date | Mar 13, 2017 |
| Decision | Substantially Equivalent |
| Regulation | 888.3030 |
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