510(k) K192117 · MQP Spinal Vertebral Body Replacement Device
Small VBR
| Applicant | Ulrich GmbH & Co. KG, Ulm, DE |
| Decision | Substantially Equivalent, Nov 1, 2019 |
| Received | Aug 6, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192117
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.