Clariance · Class II · Cleared Apr 26, 2024
| K-number | K240872 |
| Device name | Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System |
| Applicant | Clariance |
| Product code | NKB |
| Device class | Class II |
| Decision date | Apr 26, 2024 |
| 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