510(k) K250554 · QLQ Manual Instruments Designed For Use With Total Disc Replacement Devices
prodisc® L Instruments
| Applicant | Centinel Spine, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Apr 25, 2025 |
| Received | Feb 25, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250554
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.