510(k) K192214 ยท MQP Spinal Vertebral Body Replacement Device
CarboClear VBR System
| Applicant | CarboFix Orthopedics , Ltd., Herzeliya, IL |
| Decision | Substantially Equivalent, Oct 11, 2019 |
| Received | Aug 15, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192214
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.