510(k) K041888 ยท MQP Spinal Vertebral Body Replacement Device
CURVED PEEK TETRIS SPINAL IMPLANT
| Applicant | Signus Medizintechnik GmbH, Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 10, 2004 |
| Received | Jul 12, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041888
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.