510(k) K173800 · MQP Spinal Vertebral Body Replacement Device
Camber Spine Technologies SPIRA - V Open Matrix Corpectomy Cage
| Applicant | Camber Spine Technologies, Wayne PA, US |
| Decision | Substantially Equivalent, Feb 2, 2018 |
| Received | Dec 14, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173800
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.