510(k) K241332 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
aprevo® anterior and lateral lumbar interbody fusion device; aprevo® anterior lumbar interbody fusion devices with interfixation; aprevo® transforaminal lumbar interbody fusion device
| Applicant | Carlsmed, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Sep 20, 2024 |
| Received | May 10, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241332
No recall in the FDA data names this 510(k).
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