510(k) K192026 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Peridot Intervertebral body fusion System
| Applicant | Gbs Commonwealth Co., Ltd., Geumcheon-Gu, KR |
| Decision | Substantially Equivalent, Nov 26, 2019 |
| Received | Jul 29, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192026
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.