| K-number | K001476 |
| Device name | TORQUE INSTRUMENT, MODEL 8500 |
| Applicant | Spinalight, Inc. |
| Product code | LXM |
| Device class | Class U |
| Decision date | Aug 4, 2000 |
| Decision | Substantially Equivalent |
| Regulation | — |
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