510(k) K222082 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
aprevo® anterior and lateral lumbar interbody fusion devices, aprevo® transforaminal lumbar interbody fusion devices
| Applicant | Carlsmed, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Aug 12, 2022 |
| Received | Jul 15, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K222082
No recall in the FDA data names this 510(k).
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