510(k) K031757 ยท MQP Spinal Vertebral Body Replacement Device
PEEK TETRIS SPINAL IMPLANT
| Applicant | Signus Medical, LLC, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 30, 2003 |
| Received | Jun 6, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031757
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.