Nuvasive, Inc. · Class II · Cleared Nov 13, 2000
| K-number | K002677 |
| Device name | NUVASIVE INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM |
| Applicant | Nuvasive, Inc. |
| Product code | BXM |
| Device class | Class II |
| Decision date | Nov 13, 2000 |
| Decision | Substantially Equivalent |
| Regulation | 868.2775 |
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