FDA 510(k) Applications for Medical Device Product Code "BXM"
(Stimulator, Nerve, Ac-Powered)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K013215 | NUVASIVE, INC. | MODIFIED INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM | 10/16/2001 |
| K002677 | NUVASIVE, INC. | NUVASIVE INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM | 11/13/2000 |
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