The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive Navigation Instruments.
| Device ID | K172623 |
| 510k Number | K172623 |
| Device Name: | NuVasive Navigation Instruments |
| Classification | Orthopedic Stereotaxic Instrument |
| Applicant | NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 |
| Contact | Manthan J. Damani |
| Correspondent | Manthan J. Damani NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 |
| Product Code | OLO |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-01 |
| Decision Date | 2017-12-21 |
| Summary: | summary |