510(k) K162133 ยท MQP Spinal Vertebral Body Replacement Device
VerteFIT Corpectomy Cage System
| Applicant | Ldr Spine USA, Inc., Austin TX, US |
| Decision | Substantially Equivalent, May 16, 2017 |
| Received | Aug 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162133
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.