510(k) K243802 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
aprevo® anterior and lateral lumbar interbody fusion device, aprevo® anterior lumbar interbody fusion device with interfixation
| Applicant | Carlsmed, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Mar 17, 2025 |
| Received | Dec 11, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243802
No recall in the FDA data names this 510(k).
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