510(k) K221687 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Pegasus-X Expandable PLIF System
| Applicant | GS Medical Co., Ltd., Cheongju-Si, KR |
| Decision | Substantially Equivalent, Jul 27, 2022 |
| Received | Jun 10, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221687
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.