510(k) K203683 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CarboClear Lumbar Cage System
| Applicant | Carbofix Orthpedics , Ltd., Herzeliya, IL |
| Decision | Substantially Equivalent, Jan 15, 2021 |
| Received | Dec 17, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K203683
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.