510(k) K153783 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF
| Applicant | Spinevision S.A., Antony, FR |
| Decision | Substantially Equivalent, May 4, 2016 |
| Received | Dec 31, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153783
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.