510(k) K122317 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TETRIS II
| Applicant | Signus Medizintechnik GmbH, Chesterland OH, US |
| Decision | Substantially Equivalent, Aug 29, 2012 |
| Received | Aug 1, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122317
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.