510(k) K231769 · QLQ Manual Instruments Designed For Use With Total Disc Replacement Devices
activL® Next Generation Instrumentation
| Applicant | Aesculap Implants Systems, LLC, Center Valley PA, US |
| Decision | Substantially Equivalent, Jul 13, 2023 |
| Received | Jun 16, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231769
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.