Dunamis, LLC · Class II · Cleared Jul 6, 2016
| K-number | K160996 |
| Device name | Dunamis Suture Anchor PEEK 3.0mm, 3.5mm, 4.5mm, 5.5mm, 6.5mm |
| Applicant | Dunamis, LLC |
| Product code | MBI |
| Device class | Class II |
| Decision date | Jul 6, 2016 |
| Decision | Substantially Equivalent |
| Regulation | 888.3040 |
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