510(k) K232292 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Peridot-EX Expandable Intervertebral Body Fusion System
| Applicant | Gbs Commonwealth Co., Ltd., Geumcheon-Gu, KR |
| Decision | Substantially Equivalent, Nov 7, 2023 |
| Received | Aug 1, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232292
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.