510(k) K241117 · QLQ Manual Instruments Designed For Use With Total Disc Replacement Devices
M6-C Single Use, Disposable Instrumentation
| Applicant | Spinal Kinetics / Orthofix / Seaspine, Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jun 21, 2024 |
| Received | Apr 23, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241117
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.