510(k) K220782 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
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| Applicant | Alphatec Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Jun 9, 2022 |
| Received | Mar 17, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220782
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.