Trinity Orthopedics, LLC · Class II · Cleared May 21, 2007
| K-number | K070295 |
| Device name | SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM |
| Applicant | Trinity Orthopedics, LLC |
| Product code | MNI |
| Device class | Class II |
| Decision date | May 21, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 888.3070 |
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