510(k) K242869 · 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, Dec 17, 2024 |
| Received | Sep 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242869
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.