510(k) K171151 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ACRON TLIF System
| Applicant | Spinemed Ges.M.B.H, Wien, AT |
| Decision | Substantially Equivalent, Apr 27, 2018 |
| Received | Apr 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171151
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.