510(k) K072132 ยท MQP Spinal Vertebral Body Replacement Device
LDR SPINE ROI-T SYSTEM
| Applicant | Ldr Spine USA, Austin TX, US |
| Decision | Substantially Equivalent, Aug 30, 2007 |
| Received | Aug 2, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072132
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.