510(k) K212070 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
KMTI S141 Lumbar Interbody Fusion System
| Applicant | Kyocera Medical Technologies, Inc., Redlands CA, US |
| Decision | Substantially Equivalent, Aug 30, 2021 |
| Received | Jul 2, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K212070
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.