510(k) K201671 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
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| Applicant | Acuity Surgical Devices, LLC, Irving TX, US |
| Decision | Substantially Equivalent, May 4, 2021 |
| Received | Jun 19, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201671
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.