510(k) K220953 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ChoiceSpine TigerShark M, Modular Interbody System
| Applicant | Choice Spine, LLC, Knoxville TN, US |
| Decision | Substantially Equivalent, Sep 13, 2022 |
| Received | Apr 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220953
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.