510(k) K220861 ยท QLQ Manual Instruments Designed For Use With Total Disc Replacement Devices
M6-C Artificial Cervical Disc Instruments AS
| Applicant | Spinal Kinetics, LLC, Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jun 2, 2022 |
| Received | Mar 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220861
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.