510(k) K221848 ยท QLQ Manual Instruments Designed For Use With Total Disc Replacement Devices
prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments
| Applicant | Centinel Spine, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Aug 19, 2022 |
| Received | Jun 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221848
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.