510(k) K263159 · QLQ Manual Instruments Designed For Use With Total Disc Replacement Devices
prodisc® C; prodisc® C SK; prodisc® C Nova; prodisc® C Vivo Instruments
| Applicant | Centinel Spine, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Oct 7, 2026 |
| Received | Sep 9, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K263159
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.