| K-number | K193059 |
| Device name | G1 40 Radiopaque Bone Cement |
| Applicant | G21, S.R.L. |
| Product code | LOD |
| Device class | Class II |
| Decision date | Mar 19, 2020 |
| Decision | Substantially Equivalent |
| Regulation | 888.3027 |
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