510(k) K211757 ยท QLQ Manual Instruments Designed For Use With Total Disc Replacement Devices
Simplify Disc
| Applicant | Nuvasive, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Aug 20, 2021 |
| Received | Jun 7, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211757
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.