510(k) K210574 ยท OLO Orthopedic Stereotaxic Instrument
NuVasive Pulse System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Jul 29, 2021 |
| Received | Feb 26, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210574
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 3, 2023 | NuVasive Inc NuVasive MD Pulse III Multimodality System REF 1881500
Pulse Software version 369-BL.US and 369-BLN.US Open, Classified |
OLO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.