510(k) K232792 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
icotec Interbody Cage System (icotec Cervical Cage, icotec PLIF Lumbar Cage, icotec ETurn TLIF Lumbar Cage)
| Applicant | Icotec AG, 9450 Altstaetten (Sg), CH |
| Decision | Substantially Equivalent, Apr 5, 2024 |
| Received | Sep 11, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232792
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.